ECLARO
Job Number: 25-05497
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.
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
Work on routine manufacturing assignments per written procedures, recognizing deviations from accepted practice.
Adhere to Good Manufacturing Practices and standard operating procedures.
Weigh raw materials, assemble, clean, sterilize process equipment, monitor processes, complete electronic work instructions and maintain a clean room environment to comply with regulatory requirements.
Train for proficiency in primary production equipment (e.g., bioreactors, chromatography skids, media or buffer preparation equipment).
Train for proficiency in process automation systems (e.g., Delta V, Syncade, Pi Vision) and supporting business systems (e.g., SAP, Infinity, Maximo).
Assist with revision or creation of process documents such as SOPs and electronic work instructions.
Assist in maintaining materials, components, and inventory levels.
Support a safe work environment.
Qualifications
At least 1 year of experience in a GMP environment.
High school diploma required; a B.S. in science, engineering, biochemistry or related discipline is desired but not required.
Prior evidence of successful participation on work/study teams with combined contribution, collaboration, and results.
Demonstrated proficiency in common computer tools (word processing, spreadsheets, web-based applications).
Attention to detail and personal accountability critical to success.
Good interpersonal skills, attentive and approachable.
Maintains a professional and productive relationship with area management and co-workers.
Works in teams and maintains continual interaction with bioprocess teams and other departments (Quality, Materials Management, Maintenance).
Daily contact with supervisory staff for work assignments, coaching and management discussions.
Occasional contact with other line management staff regarding specific project responsibilities may be expected.
If hired, you will enjoy the following ECLARO Benefits
401(k) Retirement Savings Plan administered by Merrill Lynch
Commuter Check Pretax Commuter Benefits
Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO
If interested, please contact:
June Binuya junethel.binuya@eclaro.com 212-804-7476 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
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.
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
Work on routine manufacturing assignments per written procedures, recognizing deviations from accepted practice.
Adhere to Good Manufacturing Practices and standard operating procedures.
Weigh raw materials, assemble, clean, sterilize process equipment, monitor processes, complete electronic work instructions and maintain a clean room environment to comply with regulatory requirements.
Train for proficiency in primary production equipment (e.g., bioreactors, chromatography skids, media or buffer preparation equipment).
Train for proficiency in process automation systems (e.g., Delta V, Syncade, Pi Vision) and supporting business systems (e.g., SAP, Infinity, Maximo).
Assist with revision or creation of process documents such as SOPs and electronic work instructions.
Assist in maintaining materials, components, and inventory levels.
Support a safe work environment.
Qualifications
At least 1 year of experience in a GMP environment.
High school diploma required; a B.S. in science, engineering, biochemistry or related discipline is desired but not required.
Prior evidence of successful participation on work/study teams with combined contribution, collaboration, and results.
Demonstrated proficiency in common computer tools (word processing, spreadsheets, web-based applications).
Attention to detail and personal accountability critical to success.
Good interpersonal skills, attentive and approachable.
Maintains a professional and productive relationship with area management and co-workers.
Works in teams and maintains continual interaction with bioprocess teams and other departments (Quality, Materials Management, Maintenance).
Daily contact with supervisory staff for work assignments, coaching and management discussions.
Occasional contact with other line management staff regarding specific project responsibilities may be expected.
If hired, you will enjoy the following ECLARO Benefits
401(k) Retirement Savings Plan administered by Merrill Lynch
Commuter Check Pretax Commuter Benefits
Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO
If interested, please contact:
June Binuya junethel.binuya@eclaro.com 212-804-7476 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