Bioprocess Technician

ECLARO; Ayer (MA); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

401k Retirement Savings Plan

Medical, Dental & Vision Insurance

Job summary

A leading firm in bioprocessing is seeking a Bio Process Associate for the 2nd shift in Ayer, Massachusetts. The role involves routine manufacturing tasks, adherence to GMP, and training in the operation of production equipment. Qualified candidates should have at least 1 year of experience in a GMP environment and a high school diploma. Benefits include a 401k plan and eligibility for medical, dental, and vision insurance.

Qualifications

• 1+ year of experience in GMP environment.
• Demonstrated proficiency in common computer tools.
• Able to adhere to Good Manufacturing Practices.

Responsibilities

• Perform routine manufacturing assignments following written procedures.
• Weigh and check raw materials, and monitor processes.
• Train for proficiency in production equipment.

Skills

Attention to detail

Interpersonal skills

Team collaboration

Education

High school diploma

B.S. in science, engineering, or related discipline

Job description

Bio Process Associate - 2nd Shift

Duration: 6 months (potential extension/right to hire)

Work Schedule: Shift: 5pm-5am

Shift rotation: 3 days on (Sat, Sun, Mon), 2 days off (Tue, Wed), 2 days on (Thu, Fri), 3 days off (Sat to Mon).

Responsibilities

• Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.
• Adheres to Good Manufacturing Practices and standard operating procedures.
• Weighs and checks raw materials, assembles, cleans, and sterilizes process equipment, monitors processes, and completes electronic work instructions.
• Maintains clean room environment to comply with regulatory requirements.
• Trains for proficiency in operation of primary production equipment within the assigned functional area (bioreactors, chromatography skids, media or buffer preparation equipment, etc.).
• Trains for proficiency in process automation systems (Delta V, Syncade Interactions, Pi Vision) and supporting business systems (SAP, Infinity, Maximo, etc.).
• Assists with revision or creation of process documents such as SOPs and electronic work instructions.
• Assists in maintaining material and component inventory level.
• Supports safe work environment.

Qualifications

• Minimum 1+ year of experience in GMP environment.
• Adheres to Good Manufacturing Practices and standard operating procedures.
• High school diploma required; knowledge of science through studies resulting in a B.S., science, engineering, biochemistry or related discipline desired but not required.
• Demonstrated proficiency in common computer tools such as word processing, spreadsheet, and web‑based applications.
• Prior evidence of successful participation on work/study teams with combined contribution, collaboration, and results expected.
• Demonstrates good interpersonal skills, is attentive and approachable.
• Maintains a professional and productive relationship with area management and co‑workers.

Benefits

• 401k Retirement Savings Plan administered by Merrill Lynch
• Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro

Contact

If you feel you are qualified with the required skills and are interested, please send your most updated resume tailored to the job description above to [e-mail] or call (212)804‑7476.

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.