Quality Assurance Specialist I

A

AMPAC Fine Chemicals

Posted 3 months ago

Full Time

Rancho Cordova, California

In Person

Smart Summary

Responsibilities

The Quality Assurance Specialist I supports quality systems, coordinates cross-functional IPT meetings, and manages the release of pharmaceutical products. Key duties include conducting investigations for deviations, managing change controls, and performing facility audits to ensure GMP compliance.

Qualifications

You have an Associate's degree and 0-2 years of related technical experience in the pharmaceutical industry. You will be responsible for supporting quality systems, ensuring GMP compliance, and managing batch release processes. Strong attention to detail and the ability to work in a fast-paced, team-oriented environment are crucial.

Must Have Skills for ATS

cGMP

GMP production

document control

production record review

process validation

qualification protocols

facility audits

investigations

batch release

change controls

VAR

MNCRs

OOS/OOT investigations

QCRs

Job Description

SKpharmteco is a custom manufacturer of active pharmaceutical ingredients (APIs, Drug Substances) and registered intermediates for customers in the pharmaceutical industry. Our integrated facilities located in California, Texas, and Virginia specialize in process development, scale-up, and cGMP compliant production from kilograms to multi-ton quantities. 

We are looking for enthusiastic Quality Professionals to join our Quality Assurance Team! We have opportunities at our Rancho Cordova, CA (greater Sacramento area). 

Job Summary: 

Quality Assurance Specialist I is responsible for supporting multiple programs or supporting the coordination of the quality systems, but not necessarily both. The Quality Assurance Specialist I will be responsible for ensuring that adequate QA support is provided for the cross functional IPT meetings and customer teleconferences.  Work is closely supervised.  

Duties and Responsibilities: 

Responsible for communicating the status of QA related items to the IPT Team including batch release and investigation status

Take an active role providing, as appropriate, guidance within the approved systems and procedures as it related to GMP production and release of products, some of this guidance may be required outside of the typical working schedule (off shift)

Responsible for taking an active role in planning and execution of action items related to support of production and product release, including document control and production record review activities.

Responsible for managing the release of products to support subsequent production and release of product to customer within the approved systems and procedures

Responsible for managing change controls in support of production and release activities

Responsible for review and/or conduct of investigations for deviations in production and testing (VAR, MNCRs, OOS/OOT investigations, QCRs)

Responsible for ensuring process validation and qualification requirements are established in approved protocols and results of the validation and qualifications are adequately presented in approved reports. Responsible for facility audits of the respective manufacturing facilities at the start of each campaign and periodically while long running campaigns are active.

Responsible for ensuring that reports within a given system are progressing in a manner that complies with the approved procedures and deadlines

Responsible for ensuring submitted reports contain adequate information and attachments/links to allow appropriate review and approval

Responsible for assignment and/or reassignment of appropriate personnel to the documentation, review and approval of quality systems reports

Responsible for the development and reporting of appropriate metrics for review by management and to obtain and maintain appropriate training for the requirements of this role

EDUCATION AND EXPERIENCE

  • Associates degree required.
  • Bachelor’s degree preferred in an appropriate science.
  • 0-2 years of related technical experience or equivalent combination of education and experience.

COMPETENCIES/SKILLS

  • Strong attention to detail.
  • Ability to work in a fast paced, team-oriented environment.
  • Ability to act with a sense of urgency, while maintaining accuracy and data integrity.

CERTIFICATIONS and LICENSES

  • Not Applicable

This job description does not constitute a contract of employment or otherwise limit employment-at-will rights at any time

SKPT offers competitive salaries, benefits, and matching 401k. Our Company is an Equal Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender expression or identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics, both state and federal.

A

AMPAC Fine Chemicals

***This page has moved and is no longer active. Please follow us @SK pharmteco for all company news and updates.*** AMPAC Fine Chemicals (AFC) an SK pharmteco Company, is a United States-based, custom manufacturer of active pharmaceutical ingredients (APIs, Drug Substances) and registered intermediates. As part of the SK pharmteco group, we solve problems through technology and innovation to reliably deliver quality products that save and improve lives. With over 80 years of experience, we have mastered challenging chemistries, enabling us to provide the highest quality services to our customers. Our fully cGMP compliant facilities located in California, Texas, and Virginia specialize in process development, scale-up, and production from kilograms to multi-tonne quantities. We also have standalone contract analytical services labs. These services are conducted at AMPAC Analytical, located near our headquarters in California. State-of-the-art technology platforms include: * Commercial-scale production utilizing hazardous / energetic chemistries * High-containment facilities for the production of high-potency APIs (HPAPIs) and intermediates * Chromatographic separations using simulated moving bed (SMB) technology * Continuous processing * Controlled Substances and Specialized chemical capabilities * Analytical Laboratory Services
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