Title: QA Specialist II Risk Management
Work Location: Worcester MA 1604
Assignment Duration: 12 Months
What are the top 3-5 skills experience or education required for this position:
Hybrid Position
1. Science-related background
2. Background in GMP manufacturing
3. Experience in a QA role
4. Experience in Risk Management
5. Good Oral and written communication skills. Ability to work with cross-functional teams
Sumary
Supports activities and initiatives of the quality organisation to implement and manage the quality risk management activities as well as leading different QRM-related job tasks. This role will document evaluations relevant to commercial product risk for biologic drug substances general site risk risk associated with cross-contamination facilities utilities and equipment risk as relevant to assigned responsibilities. Working knowledge of ICHQ9 and Annexe 1 helpful.
The primary responsibilities will be collaborating with technical experts to update risk management documentation ensuring timely periodic review of risk documents and assisting in revision when appropriate.
Additional Responsibilities-
- Provide project support to the Cross Functional Team and help to facilitate risk documentation as needed for projects related to risk continuous improvement or investigations.
- Monitor and track open action items from the quality risk management activities ensuring they are implemented as required.
- Monitor periodic review obsolete documents as necessary maintain risk documentation and updates as needed.
- Analyse data from multiple sources to identify common trends and identify areas for improvement.
- Prepare reports to document the outputs of risk management monitoring activities if required.
- Escalate Risk- Use sound judgement to identify novel events new risks or changes to the risk profile make recommendations to escalate or provide a rationale why escalation is not necessary.
- Support QA Compliance activities as needed ( Investigations audits etc.)
Qualifications:
Bachelors degree in Science.
3-5 years of GMP experience preferably in Biologics risk management experience beneficial.
Effective verbal and written communication skills
Title: QA Specialist II Risk Management Work Location: Worcester MA 1604 Assignment Duration: 12 Months What are the top 3-5 skills experience or education required for this position: Hybrid Position 1. Science-related background 2. Background in GMP manufacturing 3. Experience in a QA role 4....
Title: QA Specialist II Risk Management
Work Location: Worcester MA 1604
Assignment Duration: 12 Months
What are the top 3-5 skills experience or education required for this position:
Hybrid Position
1. Science-related background
2. Background in GMP manufacturing
3. Experience in a QA role
4. Experience in Risk Management
5. Good Oral and written communication skills. Ability to work with cross-functional teams
Sumary
Supports activities and initiatives of the quality organisation to implement and manage the quality risk management activities as well as leading different QRM-related job tasks. This role will document evaluations relevant to commercial product risk for biologic drug substances general site risk risk associated with cross-contamination facilities utilities and equipment risk as relevant to assigned responsibilities. Working knowledge of ICHQ9 and Annexe 1 helpful.
The primary responsibilities will be collaborating with technical experts to update risk management documentation ensuring timely periodic review of risk documents and assisting in revision when appropriate.
Additional Responsibilities-
- Provide project support to the Cross Functional Team and help to facilitate risk documentation as needed for projects related to risk continuous improvement or investigations.
- Monitor and track open action items from the quality risk management activities ensuring they are implemented as required.
- Monitor periodic review obsolete documents as necessary maintain risk documentation and updates as needed.
- Analyse data from multiple sources to identify common trends and identify areas for improvement.
- Prepare reports to document the outputs of risk management monitoring activities if required.
- Escalate Risk- Use sound judgement to identify novel events new risks or changes to the risk profile make recommendations to escalate or provide a rationale why escalation is not necessary.
- Support QA Compliance activities as needed ( Investigations audits etc.)
Qualifications:
Bachelors degree in Science.
3-5 years of GMP experience preferably in Biologics risk management experience beneficial.
Effective verbal and written communication skills
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