Job Overview
Join a team that safeguards product quality at every step. We're looking for a meticulous, proactive Production Technician to help us deliver Paracox products with precision and care. If you thrive in GMP environments and enjoy hands‑on work with cutting‑edge equipment, we'd love to hear from you.
Responsibilities
- Blend and fill products accurately and on time, maintaining exceptional attention to detail
- Work across GMP graded environments (Grades B, C, D) and operate Grade A Restricted Access Barrier Systems
- Perform chemical sterilisation of antigens
- Clean, sterilise, and operate vessels; set up and run blending equipment and filling machines
- Prepare equipment for autoclaving; carry out routine maintenance and basic troubleshooting
- Keep precise records and documentation (including SAP tasks) in real time
- Maintain high housekeeping standards in production areas
- Support deviation investigations and periodic SOP reviews
- Own simple GMP changes and CAPA‑related tasks
- Contribute to departmental scheduling and daily planning meetings
- Provide on‑the‑job training demonstrations for new operators
- Conduct environmental monitoring and use the Laboratory Information Management System (LIMS)
What Success Looks Like
- Consistently complete batch paperwork for filled product, packing, and dispatch accurately at the point of use
- Collaborate effectively with your team while remaining confident working independently when needed
- Uphold GMP, SOPs, and safety standards without compromise; be part of a mission‑driven team producing products that make a real‑world impact
- Structured training and support from experienced colleagues
- Opportunities to grow your skills in a regulated, high‑performance environment
- 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.
Qualifications & Experience
- Experience in GMP manufacturing or sterile production environments (biopharma, vaccines, or related fields preferred)
- Comfortable working in graded cleanrooms and with barrier systems
- Skilled in equipment setup, cleaning, sterilisation, and documentation
- Familiarity with SAP and LIMS is a plus
- Strong problem‑solving mindset, reliable, and detail‑focused
- Clear communicator with a collaborative approach
Employee Status: Regular. Relocation: VISA sponsorship. Travel requirements: None. Flexible work arrangements: Not applicable. Shift: Day shift (Monday‑Friday). Valid driving license required. Hazardous material handling: Yes.
Job Posting End Date: 12/12/2025. A job posting is effective until 11:59:59 PM on the day before the listed job posting end date. Please ensure you apply no later than the day before the job posting end date.