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Pharmaceutical Production Jobs in County Durham

1 - 15 of 34
1 - 15 of 34
Search results - Pharmaceutical Production Jobs in County Durham
Tandem Project Management Ltd.-Billingham
Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or a related discipline.  •  Minimum 5 years’ experience in a biotech production support or start-up role, ideally within a GMP-regulated facility.  •  Working experience...
Hartlepool
Job Title: Process Operator - Hartlepool - Continental Salary: £27,376 per annum + £7,200 shift allowance Location: Hartlepool Reports to: Shift Supervisor / Production Management Working Hours: 06:00 - 18:00 / 18:00 - 06:00, 2 days 2 nights 4 off...
cv-library.co.uk -
Tandem Project Management Ltd.-Billingham
Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or a related discipline.  •  Minimum 5 years’ experience in a biotech production support or start-up role, ideally within a GMP-regulated facility.  •  Working experience...
SRG-Barnard Castle
Job Description Job Title: Lead, Site MSAT – Global Pharmaceutical Contract Type: Permanent Pay: competitive + bonus, car allowance, medical care, shares, pension Location: Barnard Castle Lead the Manufacturing Science and Technology (MSAT Team...
CK Group-England
Job Description CK Group are recruiting for a Senior Omnichannel Manager, to join a global pharmaceutical company, based in Uxbridge, on a contract basis for 12 months. Salary: Hourly pay up to £50.00 PAYE and inside IR35. Senior Omnichannel...
Blackfield Associates-England
Proven leadership in a production or packaging setting  •  In-depth knowledge of cGMPs and global regulatory requirements (MHRA, FDA, EU CTR)  •  Experience in clinical trial supplies or pharmaceutical manufacturing  •  Bachelor’s degree in Science...
Mane Contract Services-England
Mane are looking for an experienced Project Planner to work with their client. The client is heavily involved in Pharma, Data Center or semi conductor projects so experience in these sectors is advantageous. Responsibilities:  •  Responsible...
Blackfield Associates-England
Proven leadership in a production or packaging setting  •  In-depth knowledge of cGMPs and global regulatory requirements (MHRA, FDA, EU CTR)  •  Experience in clinical trial supplies or pharmaceutical manufacturing  •  Bachelor’s degree in Science...
SRG-Barnard Castle
Job Title: Lead, Site MSAT – Global Pharmaceutical Contract Type: Permanent Pay: competitive + bonus, car allowance, medical care, shares, pension Location: Barnard Castle Lead the Manufacturing Science and Technology (MSAT Team) for Barnard...
Morgan Latif | B Corp™-England
will play a pivotal role in steering the strategic direction, operational excellence, and cultural transformation of a facility specialising in pharmaceutical inserts and folding cartons. With annual revenues exceeding £30 million and a team of 240 talented...
Dechra Pharmaceuticals Limited-England
Job Description Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra. Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture...
Irwin and Colton - HSE Recruitment-England
Health, Safety and Environment Specialist Twickenham Salary: Circa £60,000 plus Excellent Benefits Are you ready to take the next step in your health and safety career with a leading pharmaceutical institute? Do you want to be part...
beBee Careers-England
The ideal candidate will have a strong background in pharmaceutical manufacturing, preferably in sterile or radiopharmaceutical production. You will also be required to review and certify batches in a timely manner, oversee deviations, complaints, CAPAs...
CK Group-England
support strategies and project plans, defining roles & responsibilities, timelines, and deliverables. Your Background:  •  Good understanding of industry trends including hospitality, travel, audio visual/production and technology.  •  Strong meeting...
CK Group-England
review of clinical batch records.  •  Compilation and approval of data packs and presentation to the QP for final release.  •  Conducts routine audits of data, information, procedures, equipment and systems.  •  Review and approve production and analytical...
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