QA Specialist

Croda Singapore; Alabaster (AL); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Excellent Medical, Dental, and Vision

Wellness Reimbursement

Parental Leave

Life and AD&D Insurance

Short- and long-term disability

Job summary

Croda is seeking a QA Specialist to manage GMP document control, CAPA processes, and quality data for the Quality Assurance Division in Alabaster, AL. The role supports batch releases, training programs, audits, and continuous improvement across manufacturing operations.

The ideal candidate will hold a natural sciences/engineering degree with 10–19 years in quality roles, solid FDA knowledge, and experience with GMP systems and data analysis to drive product quality and compliance.

Qualifications

• Bachelor's degree in natural sciences, engineering, or management.
• 10–19 years in quality or operations in a cGMP environment.
• Pharmaceutical operations knowledge.
• Good knowledge of FDA regulations.
• CAPA/investigation oversight experience.
• Experience collecting, analyzing, and presenting data to management.

Responsibilities

• Perform Document Control for BPRs, SOPs, RM specs, AP specs, and Job Descriptions.
• Conduct product releases/rejections including batch document reviews and specs comparisons.
• Develop and deliver GMP training programs for employees.
• Implement CAPA processes and ensure timely closure of actions.
• Oversee Facility/Equipment qualification and IQ/OQ/DQ documents.
• Conduct Annual Product Review.
• Assist during customer/FDA audits and supplier qualifications.
• Perform internal audits and review OOS documentation.
• Perform Change Control and validation program activities.

Skills

Quality Assurance

cGMP knowledge

Data analysis

CAPA investigations

Documentation control

Education

Bachelor's degree in natural sciences/engineering/related field

Tools

MasterControl

MS Excel

Job description

Croda is a FTSE 100 organisation where wetruly believeour people are our difference and this, along with our values of Innovative, Responsible and Together, creates 'our Purpose, Smart science to improve lives'. With over 5,000 employees globally, we specialise in the research and development of innovative ingredients for the Life Science and Consumer Care markets.

We are focused on developing our inclusive culture through accountability,collaborationand innovation. By joining Croda, you will be part of a team who are using smart science to create a more sustainable future.

As we deliver our ambitious 2030 Growth Strategy,we’relooking for a QA Specialist, responsible for performing duties and functions relative to maintenance of document control of GMP documents in support of Quality Assurance Division functions such as creation of documents, release of material and finished products, tracking and trending quality data, and timely escalation of quality events to management.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

WhoWe’reLooking For:

• Bachelor’s Degree required in the field of natural sciences, engineer or management preferred.
• Minimum of 10-19 years’ experience in quality or operations, primarily in a cGMP environment.
• Pharmaceutical operations experience and/or knowledge required.
• Good knowledge of FDA regulations.
• Prior CAPA / Investigation oversight experience preferred.
• Experience in collecting, analyzing, and presenting data and recommendations to management.

What You’llBe Doing:

• Perform Document Control for Batch Production Records (BPRs), Standard Operating Procedures (SOPs), Raw Material (RM), Avanti Product (AP) specifications and Job Descriptions.
• Conduct product releases/rejections including review of batch production documents, review of analytical results, and comparison to specifications.
• May be tasked with the design, development and delivery of high quality and high impact training programs and services that provide functional, GMP and product knowledge for employees to achieve a high level of performance in their jobs.
• Implement and follow the Corrective and Preventive Action Program (CAPA) process to ensure effective and timely closure of CAPAs.
• Oversight of Facility / Equipment qualification. May be required to help develop and/or review/approve User Requirements Specifications, as well as IQ/OQ/DQ documents.
• Conduct Annual Product Review.
• Provide QA input for product shipments including product release, label preparation, review and application, final label review, shipment packaging, and shipment paperwork.
• Write and revise BPRs, SOPs, RM specs, AP specs and Job Descriptions on a timely basis.
• Perform annual document reviews (when required by quality systems).
• Perform internal audits.
• Conduct raw material qualification and vendor management.
• Prepare for and assist during customer / FDA audits.
• Review / Approve Out-of-Specification (OOS) documentation.
• Perform Change Control (review and approval of Deviations and Change Requests).
• Perform process / method validation program (including design and review of validation efforts).
• May maintain or assist in the maintenance of calibration and maintenance database for equipment to ensure that equipment and instruments are fit for use.
• Keep personal training up to date using Quality Management tools provided.
• Follow all written policies delivered by Management and/or Regulatory Affairs (Standard Operating Procedures, Chemical Hygiene Plan, Emergency Contingency Plan, training memoranda, policy memoranda, Material Safety Data Sheets, Specification Records, etc.).
• Generate quality metrics using specific systems/applications by obtaining raw data, developing quality monitoring database and creating appropriate level reports using MS Excel (pivot tables, charts, graphs, etc.) or other software (MasterControl).
• Perform or participate in investigations using various tools such as root cause analysis, Failure Mode and Effects Analysis, etc.
• Assess causes systemically, looking beyond the obvious to determine why people, processes and/or systems are not meeting quality standards.
• Analyze resulting quality metrics and assess trends.
• Work with supervisors of departments to ensure consistency and close gaps in coaching and training.
• Provide ongoing analysis of data resulting from the quality systems review. Communicate results of analysis to management.
• Assist GMP work areas in developing, implementing, and maintaining On-the-Job Training (OJT) programs.
• Expected to assist in the development of junior colleagues and as assigned by QA Management, take leadership on special projects and routine activities.
• Provide new hire GMP training for employees.

Other responsibilities that are outlined in one or more different Job Descriptions may be assigned.

Physical Demands: While

performing the duties of this job, the employee is regularly required to talk, listen, hear and give instruction. This position requires normal amount of walking and standing.

Work Environment:

Requires the ability to gown and wear safety attire as well as any required protective equipment including safety glasses. Employees must meet hygiene and health requirements to allow them to work in a cGMP environment. The job function routinely works with chemicals, organic solvents and biological samples, and may on occasion require work with caustic chemicals.This job will be split between a laboratory and office setting depending on workflow and given responsibilities.

What We Offer:

• Excellent Medical, Dental, and Vision coverage, availableimmediately.
• Wellness Reimbursement
• Parental Leave
• Company paid and voluntary Life and AD&D Insurance
• Short- and long-termdisability

Additional Information:

This is a site-based rolelocatedin Alabaster, AL.

If yourequireany reasonable adjustments during the hiring process or experience any issues with our online application process, please email [e-mail].

Why Croda?

At Croda, we believe our people are our difference. We are people-led, driven by the desire to do good and deliver value, a unifying principle shaped by all the great people that have travelled through Croda since our beginning in 1925. We pride ourselves on bringing together diverse teams and talents from across the globe and, guided by our values of Responsible, Innovative, and Together, we are passionate about building an inclusive, collaborative, and diverse organisation with innovation and customer focus underpinning all that we do.

Croda recognizes employees as our strength and the diversity they bring to our workforce aredirectly linkedto our ongoing success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate based on any protected attribute, including age, race,color, religion, national origin, gender, sexual orientation, gender identity, gender expression, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law.In accordance withapplicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs.

Equal Opportunity Employer/Disability/Veterans.This Organization Participates in E-Verify