QA Document Control Specialist — GMP/Regulatory Ready
TechDigital Group
An established industry player is seeking a Quality Assurance Document Control Associate Specialist to enhance their cGMP Document Control operations. In this pivotal role, you will manage document change control processes, oversee batch records, and ensure compliance with regulatory standards. Your attention to detail and strong communication skills will be essential in collaborating with cross-functional teams and supporting internal audits. If you thrive in a fast-paced environment and are passionate about quality and continuous improvement, this opportunity is perfect for you. Join a dynamic team dedicated to excellence and innovation in document management. #J-18808-Ljbffr TechDigital Group
- ...established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP operations. In this role, you will be responsible for managing GMP records, ensuring compliance with regulatory standards, and facilitating the document approval...Regulatory
- ...established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role... ..., issuing batch records, and ensuring compliance with regulatory requirements. The ideal candidate will possess strong...Regulatory
- An established industry player is seeking a QA Associate Specialist for Document Control to support cGMP operations at their Bothell site. This role involves... ...electronic document system, ensuring compliance with regulatory standards, and collaborating with cross-functional...Regulatory
- ...Quality Assurance Document Control Specialist This position is responsible for assisting the Sr. Manager of QA in the preparing, tracking, maintaining... ...FDA, ISO 13485, and other regulatory requirements, this... ...In-depth knowledge of GMP, GDP and SOP concepts with...RegulatoryWork experience placementWork at office
- ...and supporting audits to maintain product quality. The ideal candidate will have a strong background in biotech manufacturing and regulatory compliance, with the opportunity to guide less experienced staff. Join a dynamic team committed to excellence in product quality...Regulatory
- Quality - QA Associate Specialist Document Control Job #: 4934 Pay Rate: Not Specified Job type: contractor Location... ...to receiving and reconciliation of GMP records, management of scanning,... ...knowledge of cGMPs and domestic regulatory requirements. Must complete tasks independently...RegulatoryFor contractors
$24.03 - $31.75 per hour
...Category Quality Assurance/Regulatory Affairs Position Type... ...the newest member of our QA/RA Team located in Bothell, WA... ...in failure investigations and documentation * Performs special projects... ...procedures and release in document control system * Able to describe...RegulatoryFull time- Astronics AES in Kirkland, WA is searching for a Data Management Specialist to handle technical data and controlled documents for cabin power products. You’ll collaborate with engineering, quality, and supply chain teams to ensure data accuracy and compliance. The position...Work from home2 days per week3 days per week
- Evotec is seeking a motivated Document Control Technician to join our Quality Assurance (QA) team in Redmond. This role is pivotal for ensuring that controlled... ...accurately formatted and compliant with quality and regulatory standards. The ideal candidate will have relevant...RegulatoryWork at officeFlexible hours
- ...regulations and guidelines. May assist in preparing for a hosting of regulatory and customer audits. Responsibilities: Performs general and/or... ...staff. Provides sitewide support during daily walkthroughs of GMP areas. Requirements: B.S. in Biology, Chemistry or related...Regulatory
$31 - $34.22 per hour
...records and ensuring compliance with regulations. Candidates should hold a relevant degree and have at least 2 years of experience in a GMP environment. This position requires working onsite and follows a Wednesday to Saturday schedule from 6:00 AM to 4:30 PM PST....Hourly pay$27 - $30 per hour
...Document Control Technician At Just Evotec Biologics, we believe that curiosity... ...join our Quality Assurance (QA) Team. The Document Control... ...to company quality and regulatory requirements. Responsibilities... ...What You'll Do: Format GMP documents: Apply template styles...RegulatoryTemporary workWork at officeFlexible hours- ...Responsibilities Lead QA support and... ...records and ancillary documentation to ensure accuracy... ...procedures, and readiness for disposition decisions... ...with quality and regulatory expectations.... ...oversight of change controls and periodic... ...GCP, GCLP, GLP, and GMP supplier audits with...Regulatory
- ...The ideal candidate will have over 10 years of experience in Quality, Compliance, or Regulatory roles within regulated industries. Responsibilities include leading FDA audit readiness activities, conducting gap assessments, and mentoring teams on FDA expectations. The...Regulatory
- ...Technology team. This pivotal role involves overseeing deviation records and ensuring compliance with regulatory standards. The ideal candidate will have a strong background in GMP compliance and FDA/EMA regulations, along with excellent communication and analytical skills....Regulatory
- ...highly experienced professional to lead FDA audit and inspection readiness activities. This role requires 10 years of expertise in... ...and mentor teams on compliance expectations. Strong leadership, regulatory knowledge, and excellent communication skills are essential for...Regulatory
- ...seeking a qualified professional to lead FDA audit and inspection readiness activities in Bothell, Washington. The ideal candidate will... ...with strong hands-on experience in CAPA, FDA inspections, and regulatory compliance programs. This role entails mentoring staff,...Regulatory
- ...standards. The successful candidate will engage in reviewing controlled documents, conducting quality walk-throughs, and supporting... ...quality perspective. If you are detail-oriented, possess strong regulatory knowledge, and thrive in a collaborative team environment,...RegulatoryNight shift
- An established industry player is seeking a Quality Assurance Specialist to enhance cGMP quality operations at their Bothell facility.... ...deviations, conducting investigations, and ensuring compliance with regulatory standards. The ideal candidate will possess strong...Regulatory
$25 - $34 per hour
...Health Companies Inc. in Bothell, Washington, is looking for a Documentation Analyst to administer change order processes and ensure... ...will lead meetings, manage Agile tasks, and maintain document control records. The ideal candidate is detail-oriented, has excellent...Hourly pay$164.4k - $226.05k
...Director, Quality Assurance to lead QA operations supporting GMP manufacturing of biologics. This role... ...records (deviations, CAPAs, change controls, validations). Serve as final authority... ...compliance. Represent QA in regulatory inspections, client interactions,...RegulatoryContract work- Evotec in Redmond, WA, seeks a Quality Senior Specialist Raw Material Disposition to support QC operations for biopharmaceutical manufacturing. This role is critical for ensuring regulatory compliance and quality of raw materials. Ideal candidates should have a Bachelor...RegulatoryFlexible hours
- ...FDA Audit Readiness Lead Lead FDA audit and inspection readiness... ...for FDA inspections, regulatory meetings, and compliance discussions... ...teams on FDA expectations, documentation standards, root cause... ...understanding of FDA regulations, GMP, QMS, risk management, and compliance...Regulatory
$104.63k - $161.9k
A leading medical device company in Bothell is seeking a Manager of Regulatory Compliance to oversee internal/external audits and compliance programs. This role requires a Bachelor's degree, a minimum of 3 years in a regulated environment, and strong leadership skills....Regulatory$87k - $95k
Evotec in Redmond is seeking a QA Specialist to manage quality assurance for GMP manufacturing. You will enhance QA systems and collaborate with various teams to ensure compliance. Qualified candidates should hold a bachelor's degree in a relevant field and have at least...Flexible hours- ...include the review of cGMP Controlled Documents such as SOPs, Forms, completed... .... The primary focus of the QA Associate role will be to support... ...consistent compliance with regulatory and industry expectations.... ...; provide guidance during GMP events and initiation of deviation...RegulatoryShift work
- ...Quality Assurance Specialist Location: Bothell,... ...Quality Assurance (QA) Specialist... ...completeness according to regulatory expectations. This... ...Action), change controls, process transfers... ...provide guidance during GMP events and... ...audits, including documenting observations and may...RegulatoryFor contractorsImmediate start
$92.4k - $126.5k
...Title Quality Senior Specialist Raw Material... ...Disposition - Quality Control (GMP) Location Redmond... ...commercial readiness, we’re building a... ...consistency, and regulatory compliance of raw... ...Compile lot release documentation for Product and... ...disposition meeting with QA, Manufacturing,...RegulatoryTemporary workMonday to FridayShift workDay shift$92.4k - $126.5k
...Scientist, Bioassay - Quality Control (GMP) Shifts: Day Shift, Monday-... ...and move toward commercial readiness. Responsibilities GMP... ...principles are followed in all documentation and electronic systems.... ...supporting GMP inspections and regulatory compliance. Working...RegulatoryTemporary workMonday to FridayShift workDay shift$25 - $34 per hour
...Documentation Analyst I (Aesthetics Med Device) (Bothell WA) Job Location: Bothell, Washington... ...tasks · Maintain physical document control records (e.g., DHRs), including... ...Ensure that documentation complies with GMP and regulatory requirements · Assist in development...RegulatoryHourly payTemporary workWork at officeFlexible hours
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