Manufacturing Technician

Actalent; Bedford (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

Actalent is seeking a Manufacturing Technician to operate production equipment and ensure compliance with SOPs in a cleanroom environment. The position requires proficiency in pharmaceutical manufacturing practices and an associate degree with a willingness to work in a team-oriented setting. Join a leading provider in engineering and sciences talent solutions and develop your skills in a supportive environment.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Short and long-term disability

Employee Assistance Program

Paid Time Off, Vacation or Sick Leave

Qualifications

• 0-1 years of experience in a biotech manufacturing environment.
• Ability to gown and gain entry to manufacturing areas.
• Comfortable working in a cleanroom environment.

Responsibilities

• Operate production equipment according to established procedures.
• Review manufacturing documentation for compliance.
• Coordinate sample preparation and testing.

Skills

Proficiency with SOPs

Pharmaceutical manufacturing experience

Knowledge of cell culture

Aseptic technique

Sample preparation

Good Manufacturing Practices (GMP)

Biotechnology/Pharmaceutical Manufacturing

Education

Associate degree or equivalent

Job description

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Must have experience working in a cleanroom to be considered

Job Description

Operate production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedures (OPM). Execute all procedures associated with cross-linked hyaluronic acid product production. Review manufacturing documentation for compliance. Coordinate sample preparation and testing. Record data into Batch Records, log books, and OPMs. Document all work activities according to Good Documentation Practices; recommend document revisions. Report procedural deviations and nonconformance to management.

Responsibilities

• Operate production equipment following SOPs, Batch Records, MD, and OPM.
• Execute procedures for cross-linked hyaluronic acid product production.
• Review manufacturing documentation for compliance.
• Coordinate sample preparation and testing.
• Record data into Batch Records, log books, and OPMs.
• Document all work activities according to Good Documentation Practices.
• Recommend document revisions.
• Report procedural deviations and nonconformance to management.
  
  

Essential Skills

• Proficiency with SOPs
• Experience in pharmaceutical manufacturing
• Knowledge of cell culture
• Experience with chemicals (acids, bases)
• Aseptic technique
• Sample preparation
• Good Manufacturing Practices (GMP)
• Biotechnology/Pharmaceutical Manufacturing
  
  

Additional Skills & Qualifications

• Associate degree or equivalent with biomanufacturing/pharmaceutical experience
• 0-1 years of experience in a biotech manufacturing environment
• Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas
• Comfortable working in a cleanroom environment
  
  

Work Environment

The initial training shift is from 6:00am-2:30pm Monday to Friday. After training, the shift will change to either Monday-Thursday 6:00am-4:30pm or Tuesday-Friday 6:00am-4:30pm. You will be working on the first shift with 6-8 other team members in a business casual environment. The company values hardworking, detail-oriented, and team-oriented individuals who take initiative.

Pay and Benefits

The pay range for this position is $23.25 - $23.25/hr.

Eligibility requirements apply to some benefits and may depend on your job

classification and length of employment. Benefits are subject to change and may be

subject to specific elections, plan, or program terms. If eligible, the benefits

Available For This Temporary Role May Include The Following

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
  
  

Workplace Type

This is a fully onsite position in Bedford,MA.

Application Deadline

This position is anticipated to close on Jun 5, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Management and Manufacturing

• Industries

  Business Consulting and Services

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