Associate Technician QC Microbiology and Sterility Lab Technician 2 Year Fixed Term Contract

Milton Keynes - UK

Monthly Salary: Not Disclosed

Posted on: 3 days ago

Vacancies: 1 Vacancy

Job Summary

Job Description

We have an opportunity for an Associate Technician - QC Microbiology and Sterility Lab Technician to join our team in our company.

Responsibilities:

To perform testing of intermediate and finished products in accordance with Good Manufacturing Practices (GMP) dossier and where relevant as per pharmacopoeia requirements.
Microbiology Testing (Bioburdens plate reading sterility testing Lungworm testing growth promotion and Inactivations) in accordance with Standard Operating Procedures (SOPs).
Raising of deviations in the Quality Management System and completion of non-investigative records.
Raising and completion of Deviations and CorrectiveandPreventiveAction (CAPAs).
Responsible for actioning change control tasks generated in the Quality Management System.
Entering and locking of testing result in SAP.
Update of SOPs ensuring they are current and relevant.
Completion and review of ControlofSubstancesHazardoustoHealth (COSHH) assessments.
Ensure all activities are performed in compliance with GMP our companys quality guidelines and pharmacopeia.
Update SOPs ensuring they are current and relevant to updated to minimise time taken to release batches eradicating unnecessary delays.
To upload company procedures regarding GMP and always comply with UK pharmaceutical regulations.
To comply with companys health and safety practices and procedures.

The above list of duties is not exhaustive and is subject to change. The post holder may be required to undertake other duties within the scope and grading of the post.

Your Profile:

Excellent attention to detail and ability to follow Standard Operating Procedures (SOP).
Good level of written and spoken English.
Cleanroom experience desirable.
High standard of education preferrable a degree in Chemistry or Biology or equivalent experience.
Ability to communicate with others and to work to deadlines.
Good record-keeping and a willingness to learn new skills.
Knowledge of Microsoft Office software including Excel.

Required Skills:

Accountability Accountability Bioburden Testing Biochemical Tests Biological Assessments cGMP Training Change Control Processes Compound Management Data Preparation Diagnostic Pathology Documentations GMP Compliance Growth Promotion Test Laboratory Operations Medical Testing Microbiological Techniques Microbiological Test Molecular Microbiology Pharmacokinetics Pharmacovigilance Plate Reading Policy Development Protocol Writing Quality Management Quality Management System Improvement 5 more

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Project Temps (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

Hazardous Material(s):

Yes

Job Posting End Date:

04/7/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Required Experience:

Job DescriptionWe have an opportunity for an Associate Technician - QC Microbiology and Sterility Lab Technician to join our team in our company.Responsibilities:To perform testing of intermediate and finished products in accordance with Good Manufacturing Practices (GMP) dossier and where relevant ...