Production Technician

Job Description

Production Technician

• Looking for a different challenge as a Production Technician whereby you can still utilise your skills in a manufacturing environment?
• Permanent Full-time position with competitive renumeration and benefits
• Work with a dedicated and welcoming team
• Upskill and growth in an area your passionate about, whilst being fully supported and encouraged.
• Join a Trusted Global Leading Animal Health organisation

The primary responsibility of the Production Technician is to perform day to day operations in various areas within the manufacturing department, to ensure antigen and / or vaccine is produced to required standards to meet customer demand in global markets.

The Production Technician sits within the Global Animal Health Manufacturing organization and reports to Production Manager.

What you will do:

• Operating equipment in accordance with SOPs and GMP.
• Performing tasks and processes in accordance with SOPs.
• Documenting all tasks in batch records, worksheets or logs in accordance with Good Documentation Practice (GDP).
• Maintaining good housekeeping.
• Planning daily workload.
• Communicating clearly and in a timely way with other members of the Manufacturing Team and other departments to ensure the smooth flow of product, samples and documentation.
• Perform on-the-job training for other technicians in areas of expertise.
• Contribute to continuous improvement initiatives.

Responsibilities include, however not limited to:

Minimise Deviations in the Manufacture of Product by:

• Ensuring all tasks are completed in accordance with SOPs.
• Using knowledge of processes and problem-solving techniques to thoroughly investigate and determine root cause of deviations.
• Identifying Corrective and Preventative Actions (CAPA) to eliminate further deviations occurring.
• Completing deviation reports in a timely manner.
• Implementing agreed Corrective and Preventative Actions within required timeframes.

Documentation and PV Responsibilities

• Maintain all documentation in accordance with Company and relevant quality standards.
• Review and update documentation, such as SOPs, batch records, worksheets, to ensure GMP standards continue to be met.
• Author or review assigned SOPs and documentation in required timeframes.
• Implement changes to production documents and or processes in accordance with agreed change proposals.

What You Must have

• Experience in a manufacturing environment
• Understanding of GMP
• Computer Skills: Spreadsheet, Word, SAP (desirable)
• Good time management skills
• Experience working with high standards of EHS.

What you can expect

• Work autonomously whilst being supported, encouraged and being part of a trusted, leading Global Animal Health organisation
• Exposure to upskill and develop in your role
• Joining a collaborative team of likeminded individuals
• This role requires heavy lifting and heavy physical work

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

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:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

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

Requisition ID:R343421