QC Analyst page is loaded QC Analystremote type: Onsitelocations: Grangemouth,SCtime type: Full timeposted on: Posted Todaytime left to apply: End Date: May 26, 2026 (27 days left to apply)job requisition id: R Be the First to Apply Division Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit :Job TitleQC AnalystJob DescriptionTo execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and protocols and according with best cGMP work practices, Quality standards and metricsKey Roles/Responsibilities: Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process, and final products samples and retention sample management System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department. Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents Preparation and update of SOPs, instructions and protocols and other Quality Control documentation Checking and reviewing of data in compliance with Data Integrity requirements Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives. Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Available to provide cover for other departments within the organisation as required Available to undertake any other duties as requested by the QC Manager in accordance with Company requirementsCompetencies: Attention to detail reliability effective communicationunderstanding of scientific and technical processes Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.
May 29, 2026
Full time
QC Analyst page is loaded QC Analystremote type: Onsitelocations: Grangemouth,SCtime type: Full timeposted on: Posted Todaytime left to apply: End Date: May 26, 2026 (27 days left to apply)job requisition id: R Be the First to Apply Division Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit :Job TitleQC AnalystJob DescriptionTo execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and protocols and according with best cGMP work practices, Quality standards and metricsKey Roles/Responsibilities: Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process, and final products samples and retention sample management System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department. Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents Preparation and update of SOPs, instructions and protocols and other Quality Control documentation Checking and reviewing of data in compliance with Data Integrity requirements Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives. Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical meetings and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Available to provide cover for other departments within the organisation as required Available to undertake any other duties as requested by the QC Manager in accordance with Company requirementsCompetencies: Attention to detail reliability effective communicationunderstanding of scientific and technical processes Get In TouchIntroduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.
Piramal Pharma Limited in Grangemouth is seeking a QC Analyst to execute quality control tests for raw materials and finished products in compliance with best practices and regulatory standards. Responsibilities include performing stability studies, managing QC documentation, checking data integrity, and ensuring audit readiness. Candidates should demonstrate attention to detail, effective communication skills, and a reliable work ethic, along with an understanding of GMP and safety policies.
May 29, 2026
Full time
Piramal Pharma Limited in Grangemouth is seeking a QC Analyst to execute quality control tests for raw materials and finished products in compliance with best practices and regulatory standards. Responsibilities include performing stability studies, managing QC documentation, checking data integrity, and ensuring audit readiness. Candidates should demonstrate attention to detail, effective communication skills, and a reliable work ethic, along with an understanding of GMP and safety policies.
Associate Director, Regulatory AffairsApplylocations: London,UKposted on: Posted Todayjob requisition id: R Be the First to Apply Division Piramal Critical CarePiramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs.For more details, please visit Job TitleAssociate Director, Regulatory AffairsJob DescriptionTeam lead and responsible for regulatory integration of Kenalog product line Business: Piramal Critical Care Department: Regulatory Affairs Location: London Travel: Medium Job Summary: Team lead and responsible for regulatory integration of Kenalog product line Reporting Structure: Directly reports to Director, Regulatory Affairs Key Stakeholders - Internal: Cross-Functional: Sales, Marketing, Manufacturing, Supply Chain, Medical Affairs, Quality Assurance, Quality Control, Pharmacovigilance, Planning, Program Management, Senior Management Key Stakeholders - External: Country Distributors, Health Authority (HA), external partners Essential Duties and Responsibilities Responsible for taking ownership of Kenalog marketing authorization transfer activities (MATs) and providing regulatory guidance to the global cross functional team Interpret regulations, guidelines, and compliance requirements (especially for the UK/EU region) and communicate them to other team members and functionalities/departments within the organization while demonstrating a high ability to make appropriate decisions Act as regulatory representative on multi-disciplinary product and project teams, providing advice on regulatory activities and communicates regulatory requirements to the Project Team on Kenalog MATs Develop and ensure execution of Regulatory Strategy Documents (RSDs) as required to align with business requirements Maintains up-to-date knowledge of data requirements, applicable SOPs, policies, regulations, guidelines, and industry standards Communicates with global regulatory agencies and distributors/customers as directed Assess post-approval product chemistry, manufacturing and control (CMC) changes and determine appropriate global filing strategies for Kenalog Manage the assembly, compilation, submission and electronic publishing (if required) of documentation for product compliance, registration and life cycle maintenance for Kenalog products Demonstrates excellent oral and written communication skills, including editing of documents prepared by others for regulatory submissions Lifecycle management of centralized filing documents for Kenalog Ensure global compliance of product labeling with inputs from team members Maintain regulatory files/database, chronologies and HA contact reports Participate in review and evaluation of regulatory compliance of document changes Participate in research and dissemination of issues and information to cross-functional team as necessary for Kenalog Train and mentor junior team members as required to better support business requirements Key Competencies (knowledge, skills and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Creative and able to present various solutions Energetic, enthusiastic and motivational disposition Maintain confidentiality Coaching skills Education / Experience Requires a B.S. degree in a science or related field M.S. and/or RAC preferred Knowledge of US, UK, EU, and International regulatory requirements with an emphasis on UK and EU Knowledge of Advertising and Promotional regulations highly preferred
May 29, 2026
Full time
Associate Director, Regulatory AffairsApplylocations: London,UKposted on: Posted Todayjob requisition id: R Be the First to Apply Division Piramal Critical CarePiramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs.For more details, please visit Job TitleAssociate Director, Regulatory AffairsJob DescriptionTeam lead and responsible for regulatory integration of Kenalog product line Business: Piramal Critical Care Department: Regulatory Affairs Location: London Travel: Medium Job Summary: Team lead and responsible for regulatory integration of Kenalog product line Reporting Structure: Directly reports to Director, Regulatory Affairs Key Stakeholders - Internal: Cross-Functional: Sales, Marketing, Manufacturing, Supply Chain, Medical Affairs, Quality Assurance, Quality Control, Pharmacovigilance, Planning, Program Management, Senior Management Key Stakeholders - External: Country Distributors, Health Authority (HA), external partners Essential Duties and Responsibilities Responsible for taking ownership of Kenalog marketing authorization transfer activities (MATs) and providing regulatory guidance to the global cross functional team Interpret regulations, guidelines, and compliance requirements (especially for the UK/EU region) and communicate them to other team members and functionalities/departments within the organization while demonstrating a high ability to make appropriate decisions Act as regulatory representative on multi-disciplinary product and project teams, providing advice on regulatory activities and communicates regulatory requirements to the Project Team on Kenalog MATs Develop and ensure execution of Regulatory Strategy Documents (RSDs) as required to align with business requirements Maintains up-to-date knowledge of data requirements, applicable SOPs, policies, regulations, guidelines, and industry standards Communicates with global regulatory agencies and distributors/customers as directed Assess post-approval product chemistry, manufacturing and control (CMC) changes and determine appropriate global filing strategies for Kenalog Manage the assembly, compilation, submission and electronic publishing (if required) of documentation for product compliance, registration and life cycle maintenance for Kenalog products Demonstrates excellent oral and written communication skills, including editing of documents prepared by others for regulatory submissions Lifecycle management of centralized filing documents for Kenalog Ensure global compliance of product labeling with inputs from team members Maintain regulatory files/database, chronologies and HA contact reports Participate in review and evaluation of regulatory compliance of document changes Participate in research and dissemination of issues and information to cross-functional team as necessary for Kenalog Train and mentor junior team members as required to better support business requirements Key Competencies (knowledge, skills and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Creative and able to present various solutions Energetic, enthusiastic and motivational disposition Maintain confidentiality Coaching skills Education / Experience Requires a B.S. degree in a science or related field M.S. and/or RAC preferred Knowledge of US, UK, EU, and International regulatory requirements with an emphasis on UK and EU Knowledge of Advertising and Promotional regulations highly preferred
Associate Director, Regulatory AffairsApplylocations: London,UKposted on: Posted Todayjob requisition id: R Be the First to Apply Division Piramal Critical CarePiramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs.For more details, please visit Job TitleAssociate Director, Regulatory AffairsJob DescriptionTeam lead and responsible for regulatory integration of Kenalog product line Business: Piramal Critical Care Department: Regulatory Affairs Location: London Travel: Medium Job Summary: Team lead and responsible for regulatory integration of Kenalog product line Reporting Structure: Directly reports to Director, Regulatory Affairs Key Stakeholders - Internal: Cross-Functional: Sales, Marketing, Manufacturing, Supply Chain, Medical Affairs, Quality Assurance, Quality Control, Pharmacovigilance, Planning, Program Management, Senior Management Key Stakeholders - External: Country Distributors, Health Authority (HA), external partners Essential Duties and Responsibilities Responsible for taking ownership of Kenalog marketing authorization transfer activities (MATs) and providing regulatory guidance to the global cross functional team Interpret regulations, guidelines, and compliance requirements (especially for the UK/EU region) and communicate them to other team members and functionalities/departments within the organization while demonstrating a high ability to make appropriate decisions Act as regulatory representative on multi-disciplinary product and project teams, providing advice on regulatory activities and communicates regulatory requirements to the Project Team on Kenalog MATs Develop and ensure execution of Regulatory Strategy Documents (RSDs) as required to align with business requirements Maintains up-to-date knowledge of data requirements, applicable SOPs, policies, regulations, guidelines, and industry standards Communicates with global regulatory agencies and distributors/customers as directed Assess post-approval product chemistry, manufacturing and control (CMC) changes and determine appropriate global filing strategies for Kenalog Manage the assembly, compilation, submission and electronic publishing (if required) of documentation for product compliance, registration and life cycle maintenance for Kenalog products Demonstrates excellent oral and written communication skills, including editing of documents prepared by others for regulatory submissions Lifecycle management of centralized filing documents for Kenalog Ensure global compliance of product labeling with inputs from team members Maintain regulatory files/database, chronologies and HA contact reports Participate in review and evaluation of regulatory compliance of document changes Participate in research and dissemination of issues and information to cross-functional team as necessary for Kenalog Train and mentor junior team members as required to better support business requirements Key Competencies (knowledge, skills and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Creative and able to present various solutions Energetic, enthusiastic and motivational disposition Maintain confidentiality Coaching skills Education / Experience Requires a B.S. degree in a science or related field M.S. and/or RAC preferred Knowledge of US, UK, EU, and International regulatory requirements with an emphasis on UK and EU Knowledge of Advertising and Promotional regulations highly preferred
May 29, 2026
Full time
Associate Director, Regulatory AffairsApplylocations: London,UKposted on: Posted Todayjob requisition id: R Be the First to Apply Division Piramal Critical CarePiramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs.For more details, please visit Job TitleAssociate Director, Regulatory AffairsJob DescriptionTeam lead and responsible for regulatory integration of Kenalog product line Business: Piramal Critical Care Department: Regulatory Affairs Location: London Travel: Medium Job Summary: Team lead and responsible for regulatory integration of Kenalog product line Reporting Structure: Directly reports to Director, Regulatory Affairs Key Stakeholders - Internal: Cross-Functional: Sales, Marketing, Manufacturing, Supply Chain, Medical Affairs, Quality Assurance, Quality Control, Pharmacovigilance, Planning, Program Management, Senior Management Key Stakeholders - External: Country Distributors, Health Authority (HA), external partners Essential Duties and Responsibilities Responsible for taking ownership of Kenalog marketing authorization transfer activities (MATs) and providing regulatory guidance to the global cross functional team Interpret regulations, guidelines, and compliance requirements (especially for the UK/EU region) and communicate them to other team members and functionalities/departments within the organization while demonstrating a high ability to make appropriate decisions Act as regulatory representative on multi-disciplinary product and project teams, providing advice on regulatory activities and communicates regulatory requirements to the Project Team on Kenalog MATs Develop and ensure execution of Regulatory Strategy Documents (RSDs) as required to align with business requirements Maintains up-to-date knowledge of data requirements, applicable SOPs, policies, regulations, guidelines, and industry standards Communicates with global regulatory agencies and distributors/customers as directed Assess post-approval product chemistry, manufacturing and control (CMC) changes and determine appropriate global filing strategies for Kenalog Manage the assembly, compilation, submission and electronic publishing (if required) of documentation for product compliance, registration and life cycle maintenance for Kenalog products Demonstrates excellent oral and written communication skills, including editing of documents prepared by others for regulatory submissions Lifecycle management of centralized filing documents for Kenalog Ensure global compliance of product labeling with inputs from team members Maintain regulatory files/database, chronologies and HA contact reports Participate in review and evaluation of regulatory compliance of document changes Participate in research and dissemination of issues and information to cross-functional team as necessary for Kenalog Train and mentor junior team members as required to better support business requirements Key Competencies (knowledge, skills and abilities every person must possess to be successful) Critical Thinking - using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers Excellent verbal and written communication skills Creative and able to present various solutions Energetic, enthusiastic and motivational disposition Maintain confidentiality Coaching skills Education / Experience Requires a B.S. degree in a science or related field M.S. and/or RAC preferred Knowledge of US, UK, EU, and International regulatory requirements with an emphasis on UK and EU Knowledge of Advertising and Promotional regulations highly preferred