MANUFACTURING TECH, 2nd Shift

4 weeks ago

Billerica, United States Randstad Full time

Job Title: Manufacturing Technician II (2nd Shift)

Location: Billerica, MA

Shift: 4:00 PM - 2:30 AM, Monday to Thursday

Pay Rate: $30/hr

Contract to possible perm


About the Role

We are seeking a dedicated Manufacturing Technician II to join our team in Billerica, MA. This role involves operating and maintaining essential equipment used in the production of pharmaceutical products. You will be part of a dynamic team focused on ensuring that manufacturing processes comply with cGMP, OSHA, and other regulatory requirements.

Key Responsibilities

  • Perform material transfer, preparation, batching, filling, inspection, and ancillary operations.
  • Operate automated manufacturing equipment while maintaining good aseptic technique.
  • Complete production transactions within the ERP system and ensure the accuracy of paper-based production records.
  • Coordinate the procurement of materials and manage inventory moves within the ERP system.
  • Support various functions such as equipment maintenance, engineering studies, and validation protocols.
  • Participate in safety and environmental hazard correction, actively promoting safety practices.

Essential Functions

  • Work under the direction of the manufacturing manager and team lead, with the ability to receive direction and coaching.
  • Re-prioritize work activities in a fast-paced manufacturing environment.
  • Resolve routine manufacturing problems independently or with technical group resources.
  • Communicate effectively across departments and handle pressure situations.
  • Apply knowledge of cGMP Regulations (Parts 210 and 211) and standard operating procedures (SOPs).
  • Operate computer-controlled automated production equipment and applicable software.
  • Support capital project planning, microbiology coordination, and disinfection sampling.

Basic Qualifications

  • Education:
  • Associate’s Degree in a science-related field with 1-2 years of experience in pharmaceutical/biotech manufacturing.
  • High school diploma with 3-5 years of experience in a pharmaceutical/biotech manufacturing or quality environment.
  • Experience & Skills:
  • Experience in a clean-room environment and familiarity with cGMP is preferred.
  • Hands-on experience with manufacturing equipment, troubleshooting, and process optimization.
  • Practical working knowledge of computer systems, aseptic techniques, and manufacturing processes.
  • Ability to work according to cGMP guidelines and cross-train within the organization.

Other Requirements

  • Willingness to work off-shift schedules, including holidays, weekends, and mandatory overtime as needed.
  • Active participation in promoting company values such as Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety.

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