Assoc. Tech, Quality Assurance

Job Description

The position of Associate Technician in Document Control Center (DCC) serves as Segregation of Duty (SOD) function for the site by managing the printing and issuance of controlled documents and the archival of completed GMP documentation. This role will ensure and maintain high standards of quality and compliance within our organization.   

Essential Functions and Responsibilities (Includes, but are not limited to)

The Associate Technician is responsible for:

• Print, issue and reconcile controlled documents.

• Monitor periodic review of all printed controlled documents.

• Make master cleaning batch records effective.

• Archive and retrieve GMP documentation. 

• Maintain site archived documents in the site document inventory system.

• Participate in problem-solving and continuous improvement activities.

• Perform other duties as assigned by the manager.

Qualification and Skills Requirements (Includes but are not limited to)

• Minimum “O” level certificate or Diploma in Science/ Life Science, Pharmaceutical Science, Engineering, or proven relevant experience.

• Basic knowledge of GMP and pharmaceutical regulatory requirements.

• Previous experience in quality or compliance is an advantage.

• Proficient in Microsoft office (Word, Excel).

• 1 - 3 years of relevant experience in pharmaceutical manufacturing. 

Personal Qualities

• Customer focus with continuous improvement mindset.

• Collaborative and problem-solving attitude.

• Strong communication and interpersonal skills.

• Ability to work effectively in a team environment.

Required Skills:

Accountability, Accountability, Applied Engineering, Biopharmaceutics, Communication, Continual Improvement Process, Failure Mode and Effects Analysis FMEA, GMP Compliance, Lean Manufacturing, Life Science, Microsoft Excel, Microsoft Office, Pharmaceutical Manufacturing, Pharmacology, Policy Development, Quality Assurance (QA), Quality Auditing, Quality Control Documentation, Quality Control Management, Quality Control Tools, Quality Function Deployment, Quality Improvement Programs, Quality Management, Quality Management Systems (QMS), Root Cause Analysis (RCA) {+ 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:

Temporary (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

01/30/2026

*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.