ECLARO
Bio Process Associate - 2nd Shift
Duration: 6 months (potential extension / potential 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). Must be flexible to work on holidays.
Be part of a company that delivers life‑changing healthcare solutions. ECLARO is looking for a
Bio Process Associate
for our client in
Devens, MA .
ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world.
Position Overview The Bio Process Associate / Specialist assists in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs).
Responsibilities
Works on routine manufacturing assignments per written procedures, recognizing deviations from accepted practice.
Adheres to Good Manufacturing Practices and standard operating procedures.
Weighs and checks raw materials; assembles, cleans, and sterilizes process equipment; monitors processes; completes electronic work instructions and maintains a clean‑room environment to comply with regulatory requirements.
Trains for proficiency in the operation of primary production equipment within the assigned functional area (e.g., bioreactors, chromatography skids, media or buffer preparation equipment).
Trains for proficiency in process automation systems (e.g., Delta V and Syncade Interactions, Pi Vision) and supporting business systems (e.g., SAP, Infinity, Maximo).
Assists with revision or creation of process documents such as SOPs and electronic work instructions.
Assists in maintaining material and component inventory levels.
Supports a safe work environment.
Qualifications
1+ year experience in a GMP environment.
High school diploma required; knowledge of science or related discipline (B.S. in science, engineering, biochemistry, etc.) desired but not required.
Evidence of successful collaboration on work/study teams.
Proficiency with common computer tools (word processing, spreadsheets, web‑based applications).
Experience where attention to detail and personal accountability were critical to success.
Good interpersonal skills; attentive and approachable.
Professional and productive relationship with area management and co‑workers.
Effective teamwork with bioprocess, quality, materials management, and maintenance staff.
Daily contact with supervisory staff for work assignments, coaching, and management discussions.
Occasional contact with line management staff regarding specific project responsibilities.
Benefits
401(k) Retirement Savings Plan administered by Merrill Lynch
Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO
Phone: 212-804-7476
Contact: June Binuya | LinkedIn
Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
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Duration: 6 months (potential extension / potential 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). Must be flexible to work on holidays.
Be part of a company that delivers life‑changing healthcare solutions. ECLARO is looking for a
Bio Process Associate
for our client in
Devens, MA .
ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world.
Position Overview The Bio Process Associate / Specialist assists in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs).
Responsibilities
Works on routine manufacturing assignments per written procedures, recognizing deviations from accepted practice.
Adheres to Good Manufacturing Practices and standard operating procedures.
Weighs and checks raw materials; assembles, cleans, and sterilizes process equipment; monitors processes; completes electronic work instructions and maintains a clean‑room environment to comply with regulatory requirements.
Trains for proficiency in the operation of primary production equipment within the assigned functional area (e.g., bioreactors, chromatography skids, media or buffer preparation equipment).
Trains for proficiency in process automation systems (e.g., Delta V and Syncade Interactions, Pi Vision) and supporting business systems (e.g., SAP, Infinity, Maximo).
Assists with revision or creation of process documents such as SOPs and electronic work instructions.
Assists in maintaining material and component inventory levels.
Supports a safe work environment.
Qualifications
1+ year experience in a GMP environment.
High school diploma required; knowledge of science or related discipline (B.S. in science, engineering, biochemistry, etc.) desired but not required.
Evidence of successful collaboration on work/study teams.
Proficiency with common computer tools (word processing, spreadsheets, web‑based applications).
Experience where attention to detail and personal accountability were critical to success.
Good interpersonal skills; attentive and approachable.
Professional and productive relationship with area management and co‑workers.
Effective teamwork with bioprocess, quality, materials management, and maintenance staff.
Daily contact with supervisory staff for work assignments, coaching, and management discussions.
Occasional contact with line management staff regarding specific project responsibilities.
Benefits
401(k) Retirement Savings Plan administered by Merrill Lynch
Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO
Phone: 212-804-7476
Contact: June Binuya | LinkedIn
Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
#J-18808-Ljbffr