Mackenzie Fit Recruitment is looking for Production Operatives for well known Scottish Atlantic Salmon Factory located in Rosyth, Fife. This role involves assisting with the production process, sorting and packaging fresh and smoked Salmon on production lines, ensuring food safety standards are maintained, and supporting the smooth operation of our facilities. The ideal candidate will be organised, have good attention to detail, be disciplined with good time keeping and positive, can-do attitude. Job location: Rosyth, Fife Hourly rate: 12.62. Overtime paid at 18.93 per hour and double rate at 25.24 per hour. Opportunities to become Skilled Operator at 13.03 per hour and Advanced Skilled Operator 13.34. Shift: 06:00 - 18:30 on shift 2-2-3 (two days working, two days off, two days working, two days off, three days working, two days off and so on) - Possibility of permanent contract after 12 weeks - 30 days of holidays after 12 weeks of working on site - Ongoing employment all-year-round - The basics of English will be enough for this role Having own car would be an advantage due to the location of the factory. Benefits: - Company Pension - Free parking at the factory - Employee, subsidised canteen with hot meal Immediate start is available. Apply for this role today via this website.
Mar 01, 2026
Seasonal
Mackenzie Fit Recruitment is looking for Production Operatives for well known Scottish Atlantic Salmon Factory located in Rosyth, Fife. This role involves assisting with the production process, sorting and packaging fresh and smoked Salmon on production lines, ensuring food safety standards are maintained, and supporting the smooth operation of our facilities. The ideal candidate will be organised, have good attention to detail, be disciplined with good time keeping and positive, can-do attitude. Job location: Rosyth, Fife Hourly rate: 12.62. Overtime paid at 18.93 per hour and double rate at 25.24 per hour. Opportunities to become Skilled Operator at 13.03 per hour and Advanced Skilled Operator 13.34. Shift: 06:00 - 18:30 on shift 2-2-3 (two days working, two days off, two days working, two days off, three days working, two days off and so on) - Possibility of permanent contract after 12 weeks - 30 days of holidays after 12 weeks of working on site - Ongoing employment all-year-round - The basics of English will be enough for this role Having own car would be an advantage due to the location of the factory. Benefits: - Company Pension - Free parking at the factory - Employee, subsidised canteen with hot meal Immediate start is available. Apply for this role today via this website.
We are seeking a detail-oriented and dedicated Technician to join our client's Pharmaceutical Manufacturing team. This is an Entry Level position for the candidates who recently graduated from University or College and are passionate about pharmaceutical industry. The successful candidate will be responsible for supporting manufacturing and quality control processes within a cGMP regulated environment usually in a Clean Room. This role offers an excellent opportunity for someone who wants to gain experience within highly advanced manufacturing operation and is prepared to work in a cleanroom environment and ensure compliance with cGMP regulations at all times. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience in GMP manufacturing or working in a cleanroom environment would be an advantage (but not essential) Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Good practical skills Demonstrates good literacy and numeracy skills Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Good levels of physical fitness Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Benefits Private Medical Insurance and Health Cash Plan Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking Discretional annual bonus This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please note: Only candidates with permanent Right to Work in the UK will be considered. Please email your CV today or apply through this website.
Mar 01, 2026
Full time
We are seeking a detail-oriented and dedicated Technician to join our client's Pharmaceutical Manufacturing team. This is an Entry Level position for the candidates who recently graduated from University or College and are passionate about pharmaceutical industry. The successful candidate will be responsible for supporting manufacturing and quality control processes within a cGMP regulated environment usually in a Clean Room. This role offers an excellent opportunity for someone who wants to gain experience within highly advanced manufacturing operation and is prepared to work in a cleanroom environment and ensure compliance with cGMP regulations at all times. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience in GMP manufacturing or working in a cleanroom environment would be an advantage (but not essential) Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Good practical skills Demonstrates good literacy and numeracy skills Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Good levels of physical fitness Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Benefits Private Medical Insurance and Health Cash Plan Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking Discretional annual bonus This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please note: Only candidates with permanent Right to Work in the UK will be considered. Please email your CV today or apply through this website.
We are seeking a detail-oriented and experienced Manufacturing Technician to join our pharmaceutical team. The successful candidate will be responsible for supporting manufacturing and quality control processes within a regulated laboratory environment. This role offers an excellent opportunity for someone who wants to expand experience within highly advanced pharmaceutical operation and is prepared to work in a cleanroom environment and ensure compliance with GMP regulations at all times. The ideal candidate will therefore have a pharmaceutical background and have ideally gained experience within a cGMP, FDA and MHRA regulated environment. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience of pharmaceutical manufacturing or working in a cleanroom environment Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Be flexibile - to ensure production output and client demands Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Previous GMP (Good Manufacturing Practice) experience Good practical skills Demonstrates good literacy and numeracy skills Required: Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Please note: Only candidates with permanent Right to Work in the UK will be considered. Benefits Private Medical Insurance and Health Cash Plan with Bupa Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please email your CV or apply through this website.
Mar 01, 2026
Full time
We are seeking a detail-oriented and experienced Manufacturing Technician to join our pharmaceutical team. The successful candidate will be responsible for supporting manufacturing and quality control processes within a regulated laboratory environment. This role offers an excellent opportunity for someone who wants to expand experience within highly advanced pharmaceutical operation and is prepared to work in a cleanroom environment and ensure compliance with GMP regulations at all times. The ideal candidate will therefore have a pharmaceutical background and have ideally gained experience within a cGMP, FDA and MHRA regulated environment. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience of pharmaceutical manufacturing or working in a cleanroom environment Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Be flexibile - to ensure production output and client demands Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Previous GMP (Good Manufacturing Practice) experience Good practical skills Demonstrates good literacy and numeracy skills Required: Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Please note: Only candidates with permanent Right to Work in the UK will be considered. Benefits Private Medical Insurance and Health Cash Plan with Bupa Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please email your CV or apply through this website.
