How does swipeandhired work?

You set your target roles, salary floor and locations once. swipeandhired scores matching postings against your profile, drafts tailored application materials with AI, and either lets you swipe to apply, one tap at a time, or runs fully on autopilot. Every application is tracked in your dashboard.

Which ATS platforms does swipeandhired support?

All of them. swipeandhired applies on every applicant tracking system (ATS) employers use, including Workday, SmartRecruiters, Greenhouse, iCIMS, Lever, Ashby, Taleo, SuccessFactors, Oracle Cloud and Jobvite, and on a company's own careers page when it uses none of them. You can also bring any posting yourself by link or pasted text.

Can I cancel my subscription?

Anytime, in one click from the billing portal in Settings. Your plan stays active until the end of the current billing period. No retention calls, no dark patterns.

Is my data used for training AI models?

Our platform AI provider may use the content we send it, your profile and the job posting, to improve its models. We never sell your data. If you bring your own AI provider key, requests go directly to your provider under their terms.

EXPANSION Sr. Mfg QA Specialist at Piramal Pharma, Lexington

EXPANSION Sr. Mfg QA Specialist at Piramal Pharma in Lexington. Contract. Est. up to $60k. Apply with swipeandhired.

Be the First to Apply

Division
Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit: www.piramalpharmasolutions.com
Job Title
EXPANSION Sr. Mfg QA Specialist Job Description
Business: Pharma Solutions
Department: Quality Assurance (QA)
Location: Lexington Job Overview
Reporting to the Quality Assurance Supervisor, the primary purpose of the Senior Manufacturing QA Specialist role is to perform in-process QA activities, environmental monitoring of facilities and utility systems, audits and QMS support according to Good Manufacturing Practices (GMP) and site specific Standard Operating Procedures (SOP).

Reporting Structure
This position reports to the Quality Assurance Supervisor.

Shift
Nights

Key Responsibilities:

Demonstrate strong knowledge of aseptic processing, cleanroom behavior, and cGMP requirements and consistently maintain compliance with site procedures.
Perform and provide oversight of in-process QA activities, including inspections, labeling, packaging, and line clearances in accordance with approved SOPs.
Review executed batch records, protocols, and supporting documentation to support timely and compliant batch disposition.
Perform and provide technical oversight of Environmental Monitoring (EM) activities for classified areas, including viable surface/air and non-viable air monitoring.
Perform sampling and testing of site utilities, including water, steam, and compressed gases, as applicable.
Perform microbiological testing, including plate enumeration, result review, and accurate documentation.
Support cleaning verification activities, including sample collection, testing, review, and documentation.
Maintain laboratory instrumentation and ensure required calibration and qualification activities are completed.
Evaluate EM and quality trends, identify potential adverse trends, and initiate appropriate risk-based actions and continuous improvement initiatives.
Support microbiology material and EM media inventory management to ensure testing readiness and compliance.
Prepare, review, and revise SOPs, technical reports, risk assessments, site metrics, and other QA/EM documentation.
Lead complex GMP investigations, including root-cause analysis, product impact assessments, risk assessments, and CAPA development in accordance with the site QMS.
Serve as a Senior MQA Subject Matter Expert (SME) for Environmental Monitoring, Contamination Control, Sterility Assurance, and complex manufacturing quality issues.
Support the development, implementation, and continuous improvement of the site's Environmental Monitoring and Contamination Control programs, including associated risk assessments and technical reports.
Provide senior QA oversight and coordination of quality activities supporting batch disposition and product release.
Serve as an MQA representative during client, internal, and regulatory audits, including FDA and MHRA inspections, and support responses to audit observations.
Provide technical guidance, coaching, and mentoring to MQA Specialists and serve as an escalation point for complex quality and compliance matters.
Lead and support quality and process improvement initiatives involving QA processes, QMS performance, EM, contamination control, and manufacturing quality.
Perform material disposition and associated activities in SAP, ensuring accurate documentation and timely disposition.
Participate in client interactions, investigations, technical discussions, and other site quality activities as required by management.
Ensure compliance with all applicable cGMP, regulatory, health, safety, environmental, and company requirements.

Qualifications:

Bachelor’s degree in physical or biological sciences or related scientific field preferred.
4+ years of Quality assurance or Environmental monitoring experience performing quality related activities within a pharmaceutical manufacturing environment
Must have previous experience working within QA Plant support (IPQA /EM), strict regulatory guidelines, cGMP or FDA
Prior knowledge and/or ability to understand and follow job related regulatory requirements (cGMP, OSHA, FDA)
Proficiency in the Microsoft Office applications (Word, Excel, Outlook and Access)
Demonstrated ability to effectively communicate both verbally and in writing
Ability to read and follow written instructions
Detail oriented
Understanding of sterile manufacturing preferred
Technical writing skills preferred