Top 9 Senior quality analyst Jobs in Barceloneta Pr

Senior Product Quality Assurance (PQA) Analyst
Artech LLC —Barceloneta, PR
- $38.00 - $41.43 an hour
- Contract
- 6 years
- Analysis skills
- Senior level
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3d
PQA Analyst
Kelly Services —Barceloneta, PR
- $1 an hour
- Full-time
- 6 years
- Mid-level
- Analysis skills
- Paid holidays
- Disability insurance
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2d
Senior Tax Analyst
Imperium Management Group —Dorado, PR
- $55,000 - $65,000 a year
- Full-time
- Background check
- Spanish
- CPA
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Lead - SME Plating Engineer
Eaton —Arecibo, PR
- Extended hours
- Spanish
- 5 years
- English
8d

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Artech LLC —Barceloneta, PR
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Senior Product Quality Assurance (PQA) Analyst
Artech LLC —Barceloneta, PR
During routine operations, the Senior PQA Analyst is responsible for supporting the day to day Quality Assurance activities related to the TPM plants including…
$38.00 - $41.43 an hour
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3d

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Senior Product Quality Assurance (PQA) Analyst

Artech LLC -
Barceloneta, PR

Quick Apply

Job Details

Contract
$38.00 - $41.43 an hour
3 days ago

Qualifications

Drug regulation
Pharmaceutical company experience
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

Job Title: Senior Analyst, PQA
Location: Barceloneta, PR (Onsite)
Duration: 12 Years
Pay Range: $38/hr - $41.43/hr

Job Description:
The Senior Product Quality Assurance (PQA) Analyst has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is responsible for supporting the day to day Quality Assurance activities related to the TPM plants including but not limited to approval of manufacturing direction to the production floor, review and approval of manufacturing, laboratory, and raw material investigations, assess product impact analysis and corrective and preventive action for events, review and approval of changes as applicable. The Senior PQA Analyst also is responsible to evaluate supplier change notification, monitor process track and trending, and perform annual Product Quality Reviews. This person also acts as a liaison between regulatory areas and TPM plants for regulatory submission. This function also is the primary person to audit batch records for product manufactured by TPM plants and enter required batch.

Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
"Maintains an effective liaison and cooperative relationship with other Areas including but not limited Quality, Regulatory, Technical, Supply Chain, along with the TPM sites.
"Ensures that bulk drug substance and/or drug product production at TPM sites is performed as per current good manufacturing practices, according to local procedures and as per specifications and manufacturing directions provided by QA Operations.
"Ensures TPM procedures including but not limited to raw material specification, product specification, test methods, supplier change notification, shipping, are in compliance with cGMP, policies, regulatory approvals, and Quality Technical Agreement with TPM site.
"Review and approve manufacturing directions to the production floor.
"Provide support to PQA in global projects and events to ensure intended results are achieved; including planning, risk analysis, and implementation.
"Ensures investigations of TPM plant events related but not limited to process, laboratory, raw materials are completed thoroughly and documented accurately, including adequate product impact analyses and corrective and preventive action for plant events are documented.
"Perform annual Product Quality Review according to global procedure to comply with regulatory requirements.
"Participates in Trend Review Board to monitor process track and trending.
"Participates in the Global Change Review Board (GCRB) meeting as TPM representative to evaluate global changes related but not limited to supplier change notifications, process, laboratory, and regulatory submissions that impacts all sites.
"Generates detailed change management plans related to TPM plants changes to ensure intended results are achieved; including planning, risk analysis, and implementation.

Qualifications:
List required and preferred qualifications (up to 10). Include education, skills and experience.
"Bachelor s degree preferably in Engineering or Science
"Six years of experience within the Pharmaceutical operations, preferably Biologic manufacturing process
"Knowledge of GMP regulations and standards affecting pharmaceutical products
"Comprehensive knowledge and application of business and quality concepts
"Strong analytical skills and attention to detail
"Change plan, Exception Reports, SAP and LRMS experience is highly preferred
"Proven ability to adapt communication style for a variety of modes as well as for multicultural audiences
"Strong interpersonal relations / communications skills. Ability to effectively communicate across all levels of the organization

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