Technical Manufacturing Associate
Technical Manufacturing Associate
Posted on :
28-08-2025
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1 Vacancy
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Job Description
Position Details:
Our client a world-leading Pharmaceutical Company in Andover MA is currently looking for a Manufacturing Associate to join their expanding team.
Job Title: Manufactuirng Associate / Pharma Industry
Duration: 12 months contract extendable up to 48 months
Location: Andover MA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Our client a world-leading Pharmaceutical Company in Andover MA is currently looking for a Manufacturing Associate to join their expanding team.
Job Title: Manufactuirng Associate / Pharma Industry
Duration: 12 months contract extendable up to 48 months
Location: Andover MA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Technical Manufacturing Associate
Summary:
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team.
We rely on a team of dedicated and agile members who understand the importance and impact of their role in Clients mission.
Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need when they need them.
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team.
We rely on a team of dedicated and agile members who understand the importance and impact of their role in Clients mission.
Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need when they need them.
You will be part of a multi-disciplinary team responsible for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio.
You will be part of the manufacturing team focused on mammalian bio-processing this includes and not limited to supporting the manufacturing operations team reviewing Standard Operating Procedures reviewing batch records and standard work.
As part of technical operations you will be a team member who is relied to have a good understanding of procedures techniques tools materials and equipment.
Your decision making will help you prioritize workflows based on the available resources.
You will follow standard procedures to complete tasks some of which may vary in scope sequence complexity and timing.
You will contribute to the teams success by sharing of previously acquired knowledge.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
You will be part of the manufacturing team focused on mammalian bio-processing this includes and not limited to supporting the manufacturing operations team reviewing Standard Operating Procedures reviewing batch records and standard work.
As part of technical operations you will be a team member who is relied to have a good understanding of procedures techniques tools materials and equipment.
Your decision making will help you prioritize workflows based on the available resources.
You will follow standard procedures to complete tasks some of which may vary in scope sequence complexity and timing.
You will contribute to the teams success by sharing of previously acquired knowledge.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
Responsibilities:
Manage own time and professional development be accountable for own results and begin to prioritize own workflow
Cross-functional communication with tech transfer team quality and engineering as necessary
Implement Current Good Manufacturing Practices part of GxP procedures and safe handling techniques for solid dosage processing within the continuous manufacture /PCMM work stream
Perform Upstream and Downstream operations in clinical Bio-Manufacturing
Ability to follow Standard Operating Procedures and work under minimal supervision
Identify and support continuous improvement initiatives and root cause analysis tools
Generate assist and execute documentation associated with solid dosage manufacture such as working batch record documentation in-process run sheets
Complete activities identified as Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment
Work in electronic systems including QMS Documentation Laboratory Information Management System Enterprise Resource Planning (e.g. SAP) etc.
Actively participate in shift exchange activities and communication channels
Complete training to take part in safety inspections within the facility
Understand and comply with the policies procedures and working practices of Environment Health & Safety and where necessary contribute to the review and implementation of the practices in the plant.
Manage own time and professional development be accountable for own results and begin to prioritize own workflow
Cross-functional communication with tech transfer team quality and engineering as necessary
Implement Current Good Manufacturing Practices part of GxP procedures and safe handling techniques for solid dosage processing within the continuous manufacture /PCMM work stream
Perform Upstream and Downstream operations in clinical Bio-Manufacturing
Ability to follow Standard Operating Procedures and work under minimal supervision
Identify and support continuous improvement initiatives and root cause analysis tools
Generate assist and execute documentation associated with solid dosage manufacture such as working batch record documentation in-process run sheets
Complete activities identified as Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment
Work in electronic systems including QMS Documentation Laboratory Information Management System Enterprise Resource Planning (e.g. SAP) etc.
Actively participate in shift exchange activities and communication channels
Complete training to take part in safety inspections within the facility
Understand and comply with the policies procedures and working practices of Environment Health & Safety and where necessary contribute to the review and implementation of the practices in the plant.
Minimum Qualifications:
High School Diploma or GED
A minimum of 0-3 years of experience in a related role
Demonstrated experience in a biotechnology manufacturing or laboratory environment
Operational knowledge of computerized systems
Familiarity with Production Control Systems Enterprise Resource Planning Systems and other business systems
Maintains a safe work environment
Demonstrated capability to work as a team member in a matrix development team
Excellent oral and written communication skills
Strong computer skills in Microsoft Office required especially MS Word MS Excel
Understanding of scientific principles ability to think critically and demonstrate troubleshooting and problem-solving skills.
High School Diploma or GED
A minimum of 0-3 years of experience in a related role
Demonstrated experience in a biotechnology manufacturing or laboratory environment
Operational knowledge of computerized systems
Familiarity with Production Control Systems Enterprise Resource Planning Systems and other business systems
Maintains a safe work environment
Demonstrated capability to work as a team member in a matrix development team
Excellent oral and written communication skills
Strong computer skills in Microsoft Office required especially MS Word MS Excel
Understanding of scientific principles ability to think critically and demonstrate troubleshooting and problem-solving skills.
Preferred Qualifications:
Bachelors Degree
Knowledge of cell culture and or downstream processing techniques in a manufacturing setting preferred
Mechanical aptitude and desire to execute hands-on manual labor
Bachelors Degree
Knowledge of cell culture and or downstream processing techniques in a manufacturing setting preferred
Mechanical aptitude and desire to execute hands-on manual labor
Location/Schedule:
This is fully onsite role in Andover MA
Monday - Friday; 7 AM - 3:30 PM (weekend OT optional)
This is fully onsite role in Andover MA
Monday - Friday; 7 AM - 3:30 PM (weekend OT optional)
Employment Type
Full-time
Key Skills
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