QC Chemical Compliance Specialist

Pfizer; Indonesia; On-site; IDR 300.000.000 - 400.000.000; Full time

Job summary

A global pharmaceutical company in Indonesia is seeking a laboratory compliance specialist. This role involves managing laboratory documentation, ensuring compliance with quality standards, and validating methods. The ideal candidate holds a Bachelor's degree in Chemistry or Pharmacy and has experience in analytical method development. Strong analytical thinking and communication skills are essential for this position, which is based on-site. Join us in our commitment to quality and patient safety.

Qualifications

• Minimum 1 year experience in analytical method development or validation preferred.
• Strong knowledge about analytical instruments and current compendia.
• Ability to work well independently or as part of a team.

Responsibilities

• Manage compendia compliance and laboratory documentation.
• Prepare analytical method validation protocols and reports.
• Assist in writing/updating SOPs in QC Chemical Lab.

Skills

Analytical method development

Knowledge of regulatory compliance

Good analytical thinking

Interpersonal skills

Communication skills

Education

Bachelor's Degree in Chemistry or Pharmacy

Tools

Analytical instruments

Job description

Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

Your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations.

As laboratory compliance specialist, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.

It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

The role is accountable to manage compendia compliance, laboratory documentation, method validation/verification activities, and ensure that current GMP practice in QC Laboratories comply against Pfizer Quality Standard/cGMP, not limited to:

• Assist QC Manager and/or QC Lab Compliance Supervisor for writing or updating Standard Operating Procedure (SOP) and Standard test procedures (STP) in accordance with actual practices, PQS, current GMP, and regulatory requirements, in QC Chemical Lab
• Execute the project (i.e method validation/verification, etc.) in QC Laboratory Compliance Team in the most effective way and meet the target date
• Prepare analytical method validation/verification protocol and report, and study in QC Chemical area
• Support QC Lab Compliance Supervisor to manage and maintain the implementation of compendia compliance in QC Chemical
• Ensure compliance in Quality and Safety by such as submitting safety incident and CAPA as per commitment date
• Maintain QC Laboratory documentation (including registration dossier related to laboratory document) in QC Chemical Lab
• Support QC Operation team in laboratory investigation in case of out of specification
• Ensure all reagent, reference standards, and equipment are ready for testing
• Perform training to QC Lab personnel, as required

Qualifications

Must-Have

• Bachelor's Degree (Chemistry or Pharmacy)
• Min 1 year experience in analytical method development/validation will be preferred
• Strong knowledge about analytical instruments and various test procedure, including as in most current compendia (FI, USP, BP, etc.)
• Knowledge of regulatory compliance requirements for Pharmaceutical manufacturing
• Good analytical thinking and high-level integrity
• Able to work well either as an individual or as a team member
• Excellent interpersonal and communication skills

Nice-to-Have

• Good knowledge of dossier and product registration process

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.