Lead QA Specialist

Croda Singapore; Alabaster (AL); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Wellness Reimbursement

Parental Leave

Life Insurance

Disability Insurance

Job summary

Croda, a global life sciences company based in Alabama, is seeking a Lead QA Specialist to own document control for GMP and QA activities at the Alabaster site. You will manage batch records, SOPs, CAPA investigations, data analysis and prepare for customer and FDA audits, collaborating across QA, manufacturing and quality systems.

The role requires knowledge of cGMP and FDA regulations, strong communication, project leadership, and attention to detail to ensure compliance and continuous

Qualifications

• Bachelor’s degree with ≥6 years in QA or associate degree with ≥10 years.
• Knowledge of cGMP and FDA regulations preferred.
• Strong data analysis and presentation skills; high attention to detail.

Responsibilities

• Perform Document Control for BPRs, SOPs, RM specs, AP specs and Job Descriptions.
• Conduct product releases/rejections including review of batch docs and analyses against specs.
• May design and deliver high quality training programs providing GMP/product knowledge.
• Implement CAPA process and ensure timely closure of CAPAs.
• Oversee Facility/Equipment qualification and IQ/OQ/DQ documents.
• Provide QA input for product shipments and release, labeling, and paperwork.
• Write and revise quality documents on a timely basis.
• Perform annual document reviews and internal audits.
• Conduct raw material qualification and vendor management.
• Assist during customer/FDA audits and Change Control processes.
• Perform process/method validation and calibration maintenance.

Skills

Document control

Data analysis

Quality systems

GMP knowledge

Communication skills

Project management

Team collaboration

Excel

Education

Bachelor’s Degree in a relevant field

Associate's degree with 10+ years experience

Tools

Word

Excel

Outlook

MasterControl

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 Lead 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, review of analytical data and relative documents, compiling reports, release of material and finished products, tracking and trending quality data, and timely escalation of quality events to management.

WhoWe’reLooking For:

• Bachelor’s Degree with a minimum of 6 years of experience in an applicable field or associate’s degree with a minimum of 10 years of experience in an applicable field.
• Knowledge of cGMP preferred.
• Knowledge of FDA regulations preferred.
• Prior CAPA / Investigation oversight experience preferred.
• Experience in collecting, analysing, and presenting data and recommendations to management.
• Effective written and verbal communication skills required.
• Proficient in basic applications such as Word, Excel, Outlook.
• High attention to detail.
• Good command of the English language.
• Excellent organisational ability.
• Work collaboratively with others.
• Ability to manage and lead projects assigned by QA Management.
• Able to manage multiple priorities and follow through on projects to completion.
• Ability to work well in a team‑oriented environment.

WhatYou’ll Be 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 programmes 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 Programme (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.
• 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.
• Perform Change Control (review and approval of Deviations and Change Requests).
• Perform process / method validation programme (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.
• Analyse 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) programmes.
• 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 occasionally required to interact with other employees, customers, or vendors and must do so in a manner least obstructive to the conduct of business. The position is active and requires standing, walking, bending, kneeling, and stooping all day. This position requires the ability to climb stairs and lift approximately 50 lbs.

Work Environment:

Requires the ability wear all required protective equipment including safety glasses. Employees must meet hygiene and health requirements.

What We Offer:

The successful candidate will receive a competitive salary and benefits package including:

• 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 recognises 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.