Technical Associate, Clinical Manufacturing - Andover, MA

VetJobs

Andover (MA)

On-site

USD 33,000 - 55,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Benefits offered by this job

401(k) plan with Pfizer matching
Health benefits

Job summary

Pfizer is seeking an On-site Manufacturing Technician in Andover, MA. You will contribute to team deliverables, coordinate with cross-functional teams, and follow standard procedures to complete tasks within defined timelines.

You will engage in process improvements, ensure quality, and perform operator care on complex equipment while maintaining accurate batch records and documentation.

Qualifications

  • High School Diploma or GED with 2+ years of relevant experience.
  • Biotechnology manufacturing or laboratory experience.
  • Familiarity with Production Control Systems and ERP systems.

Responsibilities

  • Contribute to team deliverables and coordinate with team members.
  • Manage personal time and professional development; be accountable for results.
  • Follow procedures to complete tasks within set time frames.
  • Identify and solve moderately routine problems.
  • Complete assignments with moderate supervision and refer deviations to supervisor.
  • Ensure work accuracy, quality, and standards adherence.
  • Engage cross-functionally with tech transfer, quality, and engineering; support improvement via root cause analysis.
  • Implement cGMP practices and safe handling for solid dosage processing.
  • Perform operator care tasks for complex pharmaceutical equipment.
  • Generate and maintain batch records and in-process run sheets.

Skills

Teamwork
Communication skills
Microsoft Office

Education

High School Diploma or GED

Tools

Microsoft Office Suite

Job description

Job Description

Job Description

Job Description

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience,

Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

Use Your Power for Purpose

Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.

What You Will Achieve
In This Role, You Will

Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.

Manage personal time and professional development, being accountable for results.

Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.

Identify and solve moderately routine problems.

Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.

Ensure work is reviewed for accuracy, quality, and adherence to standards.

Engage in cross-functional communication with the tech transfer team, quality, and engineering as needed, and support continuous improvement initiatives using root cause analysis tools.

Implement Current Good Manufacturing Practices (part of GxP) and safe handling techniques for solid dosage processing within the continuous manufacture/PCMM work stream.

Perform Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment.

Generate, assist, and execute documentation related to solid dosage manufacture, including working batch record documentation and in-process run sheets.

Auto req ID

481489BR

Minimum Education Required

High School/GED

Additional Qualifications/Responsibilities

Here Is What You Need (Minimum Requirements)

  • High School Diploma or GED with 2+ years of relevant experience
  • Demonstrated experience in a biotechnology manufacturing or laboratory environment
  • Operational knowledge of computerized systems
  • Familiarity with Production Control Systems, Enterprise Resource Planning Systems, and other business systems
  • Demonstrated capability to work as a team member in a matrix development team
  • Excellent oral and written communication skills
  • Proficiency in Microsoft Office Suite
Bonus Points If You Have (Preferred Requirements)
  • Solid understanding of fermentation and downstream processing techniques
  • Experience with cGMP production of phase I/II clinical drug substances
  • Experience in commissioning and qualifying process equipment
  • Ability to execute microbial upstream and downstream processes
  • Strong problem-solving skills
  • Strong organizational skills and attention to detail
  • Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity
Physical/Mental Requirements
  • Must be able to climb flights of stairs, and remain standing for extended periods of time.
  • Must be able to lift up to 50 lbs
  • Ability to thrive in dynamic team environment with diverse perspectives
Non-standard Work Schedule, Travel Or Environment Requirements

Ability to work nights and weekends as needed depending upon process needs; nonroutine.

Work Location Assignment: On Premise

The salary for this position ranges from $24.22 to $40.36 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Massachusetts - Andover location.

City

Andover

State

Massachusetts

Job Category

Technician

Job Code

Manufacturing Manufacturing

Affiliate Sponsor

Pfizer

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Senior Process Technician - Andover, MA
Senior Process Technician - Andover, MA

VetJobs • Andover (MA)

On-site
USD 37,000 - 62,000
Production Technician II
Production Technician II

Pfizer • Town of Middleton (WI)

Hybrid
USD 62,408,000 - 104,014,000
401(k) plan with Pfizer Matching/Conpr
Pfizer Retirement Savings Contribution
Paid vacation
+3
Quality Compliance Specialist
Quality Compliance Specialist

Pfizer • Rocky Mount (NC)

On-site
USD 69,000 - 114,000
401(k) with Pfizer Matching Contributi
Paid vacation
Manager
Manager

Pfizer Belgium • Groton (CT)

On-site
USD 99,000 - 165,000
401(k) plan with Pfizer Matching
Paid vacation
Health benefits (medical, dental, vis
+1
Quality Compliance Specialist
Quality Compliance Specialist

Pfizer, S.A. de C.V • Rocky Mount (NC), Northern (KY)

Hybrid
USD 69,000 - 114,000
401(k) with Pfizer match
Pfizer Retirement Savings Contribution
Paid vacation, holidays, and personal;
+3
Quality Compliance Specialist
Quality Compliance Specialist

Biopharma Careers • Rocky Mount (NC)

On-site
USD 69,000 - 114,000
401(k) with Pfizer Matching Contrib
Paid vacation and holidays
Medical, dental and vision coverage
Sr. Maintenance Compliance Engineer
Sr. Maintenance Compliance Engineer

Pfizer • Michigan

On-site
USD 83,000 - 138,000
401(k) match
Retirement plan
Paid vacation
+3
Senior Associate Scientist, Upstream Process Development — Bioprocess Automation & Digitization
Senior Associate Scientist, Upstream Process Development — Bioprocess Automation & Digitization

Pfizer • Andover (MA)

On-site
USD 69,000 - 114,000
Manager, Process Performance Qualification
Manager, Process Performance Qualification

Pfizer • McPherson (KS)

On-site
USD 106,000 - 177,000
Relocation assistance
Hybrid work arrangement
Manager, Process Engineering - Sterile Inspection
Manager, Process Engineering - Sterile Inspection

Pfizer • Michigan

On-site
USD 99,000 - 165,000
401(k) with Pfizer Matching
Health benefits
Paid vacation & holidays
+1