Quality Assurance Senior Associate Biopharma JP10382
Quality Assurance Senior Associate Biopharma JP10382
Posted on :
16-03-2025
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1 Vacancy
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Monthly Salary
$ 28 - 32
Vacancy
1 Vacancy
Posted on :
16-03-2025
Job Description
Job Title:Quality Assurance Senior Associate Biopharma (JP10382
Location:Thousand Oaks CA. 91320
Employment Type: Contract
Business Unit:Drug Product Quality Assurance
Duration:12 months with likely extensions
Rate: $2832/Hr W2.
Posting Date:06/07/22
3 Key Consulting is hiring aQuality Assurance Senior Associatefor a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
This position supports Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision the role provides support and compliance oversight to Manufacturing and Facilities & Engineering staff in the of their processes procedures and use of quality systems. Duties include purposeful presence on the shop floor electronic batch record creation batch record review SOP revision approval work order approval and quality approval of minor deviations and CAPA records. Responsibilities will include evaluation of compliance issues providing recommendations and assuring progress of quality records to completion. The Sr. Associate will also represent functional area quality for the Drug Product Quality Assurance department in the of projects necessary to achieve departmental operational goals and will work in a team matrix environment.
Preferred Qualifications:
Masters degree and 1 years of Quality experience OR
Bachelors degree and 2 years of Quality experience OR
Associates degree and 6 years of Quality experience
Why is the Position Open
Supplement additional workload on team.
Top MustHave Skill Sets:
Day to Day Responsibilities:
The person in this role will oversee a drug product facility and interacts with different departments outside of manufacturing
Red Flags:
Minimal to no experience
Interview process:
Phone screening followed by panel interview.
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this position please feel free to take a look at the other positions on our websitewww.3keyconsulting/careers. You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role.
Location:Thousand Oaks CA. 91320
Employment Type: Contract
Business Unit:Drug Product Quality Assurance
Duration:12 months with likely extensions
Rate: $2832/Hr W2.
Posting Date:06/07/22
3 Key Consulting is hiring aQuality Assurance Senior Associatefor a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
This position supports Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision the role provides support and compliance oversight to Manufacturing and Facilities & Engineering staff in the of their processes procedures and use of quality systems. Duties include purposeful presence on the shop floor electronic batch record creation batch record review SOP revision approval work order approval and quality approval of minor deviations and CAPA records. Responsibilities will include evaluation of compliance issues providing recommendations and assuring progress of quality records to completion. The Sr. Associate will also represent functional area quality for the Drug Product Quality Assurance department in the of projects necessary to achieve departmental operational goals and will work in a team matrix environment.
Preferred Qualifications:
- Bachelors Degree in Biochemistry Biology Chemistry or related science field.
- Demonstrated ability to perform GMP operations including following detailed SOPS maintaining training and good documentation practices.
- Experience managing projects through to completion meeting timelines.
- Evaluating documentation and operations according to company procedures.
- Experience working with Quality Systems Strong organizational skills and ability to manage multiple tasks at one time Effective communication skills (both written and verbal)
- Demonstrated ability to work as both a team player and independently
- Display leadership attributes and drive improvement initiatives.
- Solid understanding and application of aseptic behaviors and principles
Masters degree and 1 years of Quality experience OR
Bachelors degree and 2 years of Quality experience OR
Associates degree and 6 years of Quality experience
Why is the Position Open
Supplement additional workload on team.
Top MustHave Skill Sets:
- Must have Pharma industry experience
- Experience in manufacturing or quality fields within biotech or pharma industries.
- Complex decision making skills ability to complete tasks autonomously provide updates to area manager and identify potential issues.
- Technical writing skills
- The ideal candidate would have applicable drug substance/drug product biotech manufacturing facilities as a QA or from a manufacturing background
Day to Day Responsibilities:
- The role provides support and compliance oversight to Manufacturing and Facilities & Engineering staff in the of their processes procedures and use of quality systems.
- Duties include purposeful presence on the shop floor electronic batch record creation batch record review SOP revision approval work order approval and quality approval of minor deviations and CAPA records.
- Responsibilities will include evaluation of compliance issues providing recommendations and assuring progress of quality records to completion.
- The Sr. Associate will also represent functional area quality for the Drug Product Quality Assurance department in the of projects necessary to achieve departmental operational goals and will work in a team matrix environment.
The person in this role will oversee a drug product facility and interacts with different departments outside of manufacturing
Red Flags:
Minimal to no experience
Interview process:
Phone screening followed by panel interview.
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this position please feel free to take a look at the other positions on our websitewww.3keyconsulting/careers. You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role.
Regards
3KC Talent Acquisition Team
Required Experience:
Senior IC
Employment Type
Full Time
Key Skills
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