Are you a detail-oriented QC Analyst with strong experience in cGMP environments and a passion for quality control in the life sciences? We are seeking a dedicated Manufacturing Technician I for a critical 1st Shift role in Framingham, MA. This is an exciting chance to join a major player in the biotechnology and pharmaceutical space, contributing directly to product quality and process integrity. The team you'd be joining has a commitment to Quality, Delivery, Cost, and Innovation, and the work you do will be essential to maintaining their high standards.
This role provides a fantastic opportunity to leverage your laboratory skills, spending approximately 80% of your time in the lab performing essential testing, sampling, and preparation duties. You will be instrumental in the quality control process, from raw material inspection to final product release. You'll be working in a state-of-the-art facility with a team that values precision and adherence to strict quality guidelines. If you are looking to make an immediate impact in a fast-paced, highly regulated industry, this is the role for you.
location: Framingham, Massachusetts
job type: Contract
salary: $34.00 - 35.76 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Perform routine testing of raw materials, in-process, and final products following standard operating procedures (SOPs).
- Collect all required samples (environmental monitoring and utilities) within specified frequencies in cGMP areas.
- Manage material preparation for the manufacturing process, including glassware washing, transfer assembly preparation, and autoclaving.
- Participate in QDCI (Quality, Delivery, Cost, and Innovation) daily meetings to review schedules and assigned testing/assays.
- Conduct data review and preliminary evaluation of results for quality procedures.
- Provide input to the technical composition of operating documentation.
- Troubleshoot minor issues by following predetermined options, such as repeating assays.
qualifications:
Required Skills & Experience
- Bachelor's Degree in the Life Sciences (i.e., Chemistry, Biology, etc.).
- 1-3 years of experience as a QC Analyst.
- MUST HAVE: Experience with the Perkin Elmer Spectrometer LAMBDA 365+.
- MUST HAVE: Proficient in Good Documentation Practices (GDP), including familiarity with ALCOA principles (Attributable, Legible, Contemporaneous, Original, and Accurate).
- Experience working in a cGMP environment.
- Familiarity with the QDCI (Quality, Delivery, Cost, and Innovation) framework.
- Experience in sample collection for environmental monitoring and utilities.
- Ability to aid in the development of test methods.
- Strong adherence to SOPs and quality guidelines.
skills: Quality control, SOP, Quality Assurance, GMP (Good Manufacturing Practice), Good Documentation Practices (GDP)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
