Manufacturing Associate

ECLARO; Devens (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player in pharmaceutical manufacturing is seeking a Bio Process Associate for the 2nd shift. This role involves operating control systems in a Biotechnology Pilot Plant, preparing process buffers, and ensuring compliance with stringent cGMP standards. The ideal candidate will possess a high school diploma and have at least five years of process operations experience, with a keen attention to detail and a commitment to teamwork. If you're ready to embrace a dynamic role in a fast-paced environment, this opportunity is perfect for you.

Qualifications

• 5+ years of process operations experience required.
• High school diploma is mandatory; A.A.S. or B.S. preferred.

Responsibilities

• Operate control systems in Biotechnology Pilot Plants.
• Prepare process buffers and reagents, ensuring compliance with cGMP.
• Communicate operational status to management timely.

Skills

Attention to Detail

Mechanical Aptitude

General Chemistry Knowledge

Mathematics Skills

Microbiology Knowledge

Team Player

Education

High School Diploma

A.A.S. or B.S. Degree

Job description

Title: Engineering - Bio Process Associate - 2nd Shift

Primary Recruiter: Jane Bautista

Pay Rate:: $38/Hour

# of Openings: 4

Schedule: Shift rotation: Shift: 5p- 5a 3 days on (Sat, Sun, Mon), 2 days off (Tues, Wed), 2 days on (Thurs, Fri), 3 days off (Sat to Mon).

Job Responsibilities:

• Operates control systems and processes in Biotechnology Pilot Plants as assigned.
• Prepares process buffers and reagents.
• Cleans equipment and maintains area in a clean and orderly fashion.
• Recognizes and reports safety, maintenance and operational variances to area management.
• Communicates status of operations to area management in a timely manner.
• Follows detailed SOPs and batch records.
• Ensures compliance with cGMP and safety requirements.
• Maintains files, records and equipment.
• Records data, logs activities and monitors processes.
• Achieves and maintains proficiency through training.

Education/Skills:

• The successful candidate will have a high school diploma with a minimum of 5 years process operations experience; A.A.S. or B.S. degree is preferred.
• Prior job-related experience required along with demonstrated mechanical aptitude.
• Familiarity with general chemistry, mathematics, microbiology, and cGMP clean room operations is a plus.
• Keen attention to detail.
• Prior experience following and documenting written instructions is required.
• Committed team player prepared to work in and embrace a team-based culture.
• Shift work and overtime required.

Additional Information:

• Work in a cGMP laboratory and/or manufacturing environment following techniques which require one to maintain a high attention to detail. Properly use Personal Protective Equipment (PPE), gowning for restricted areas, aseptic processing, handling chemicals, and work in a general office environment.
• Contingent Workers whose jobs involve the operation of a vehicle or machinery, or physical presence in a laboratory, research, drug development, or manufacturing facility are prohibited from having any amount of alcohol or illicit drugs in their body while in the workplace or performing their job functions.
• Suppliers and the Contingent Worker are responsible for ensuring they are fit for all the duties of the job.

Seniority Level

Associate

Employment Type

Contract

Job Function

Manufacturing

Industries

Pharmaceutical Manufacturing and Biotechnology Research