Quality Analyst

Kelly Services; Barceloneta (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

Kelly Services is seeking a Quality Analyst in the Barceloneta, PR area to implement and maintain the Quality System and support manufacturing operations. You will review investigations, perform risk assessments, and ensure product disposition aligns with regulatory requirements.

The ideal candidate has a Bachelor's in a relevant science, 4 years in pharma/biotech quality, and fluency in English and Spanish.

Qualifications

• Bachelor's degree in biotechnology, biology, chemistry or engineering; master's preferred.
• 4 years experience in pharmaceutical/biotechnology industry.
• Knowledge of GMP and safety regulations; quality/compliance management.
• Excellent written and spoken English and Spanish.

Responsibilities

• Support routine operations to meet quality goals and ensure compliance with Customer policies and applicable regulations for the Quality areas under responsibility. Serve as backup for the QA Manager leading the team and providing support to quality initiatives.
• Investigations of plant events are evaluated in a timely manner; documented in the plant CAPA system.
• Performs product impact analyses for plant events and places product on QA hold where appropriate.
• Participates on the Validation Review Board; approves SOPs, change management and risk management documents; ensures documents comply with global procedures and regulatory requirements.
• Approves calibration requests, calibration out of tolerance and preventive maintenance records with proper justifications.
• Demonstrates accountability and responsibility of EHS performance and compliance.
• Maintains liaison with other Quality areas and Plant departments.
• Oversees manufacturing operations to align with approved procedures.
• Support the Compliance team during internal and external audits.
• Provide guidance for new product introduction activities and develop risk assessments to support manufacturing for new products.
• Conform to EHS management system requirements and promote continuous improvement; comply with all EHS procedures and policies.
• Other program applicable according to position duties.

Skills

GMP knowledge

Quality/compliance management

English and Spanish communication

Investigations / Risk management

Education

Bachelor's degree in biotechnology, biology, chemistry or engineering

Masters degree in science preferred

Job description

AtKelly® Science, Engineering, Technology & Telecom (SETT), we’re passionate about helping you find a job that works for you. How about this one?
We’re seeking anQuality Analystto work with one of our top global biopharmaceutical clients in theBarceloneta PRarea. With us, it’s all about finding the job that’s just right

Purpose

Responsible for implementing and maintaining the effectiveness of the Quality System. Support manufacturing operations in the resolution of events, impact assessment and documentation discrepancies.
Provide guidance for product/process impact analysis, perform holistic evaluation of events, review and approve investigations and risk-based evaluations in support to routine operations and product disposition.

Responsibilities :.

• Support routine operations to ensure that all quality goals are met, and all practices and procedures comply with Customer policies and applicable regulations for the Quality areas under responsibility. Serve as backup for the QA Manager leading the team and providing support to quality initiatives.
• Ensures investigations of plant events are evaluated in a timely manner; completed thoroughly and documented accurately in the plant CAPA system.
• Performs product impact analyses for plant events and places product on QA hold where appropriate.
• Participates on the Validation Review Board as the Manufacturing Quality Assurance function. Approves standard operating procedures; change management and risk management documents. Ensures all documents are in compliance with Customer global procedures and regulatory requirements.
• Approves calibration requests, calibration out of tolerance and preventive maintenance records. Ensures that these documents have appropriate justifications according to product /process limits established.
• Demonstrates accountability and responsibility of EHS performance and compliance.
• Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.
• Oversees manufacturing operations to ensure practices are in alignment with approved procedures.
• Provide support to the Compliance team during internal and external audits as required.
• Provide guidance for new product introduction activities. Develop risk assessments to support manufacturing activities for new products and ensure material control until regulatory approval.
• Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any
• other program applicable according to the position duties.

Qualifications

• Bachelor's degree in biotechnology, Biology, Chemistry or Engineering. Masters Degree in Science preferred.
• Four (4) years of experience in Pharmaceutical/Biotechnology industry in a similar position.
• This position requires knowledge of quality / compliance /Investigations /Risk management as well as regulations and standards affecting biological products.
• Excellent written and spoken communication skills in English and Spanish.
• Knowledge of GMP, safety regulations.
• Quality/compliance management skills.
• Fast paced and adaptable to continuously changing environment. Subject to work with multiple priorities and interruptions and under reasonable pressure due to the nature and function of the area.
• Assures the quality of manufactured products and processes per standard operating processes (SOP'S) and GMP (Good Manufacturing Practices). BS degree or 3-5 years equivalent experience.

Daily Work Schedule Expectations

ALL candidates must be available for any shift/weekend/holidays.
Associate Rotating shift - 4 days at 10hours
2 months rotation on each shift 1st, 2nd, 3rdshift
Area worked based in manufacturing schedule of 24/7

Is overtime offered or required?

Must be available to work OT based in business needs