QC Specialist II

SGS_JOB_2313

Scientific
 California
Quality control

Contract - 06 months

Location : Vacaville CA Under moderate supervision, QC Specialist is expected to support planning, managing, and executing projects related to the product portfolio for Vacaville Quality Control. These projects include analytical transfers, control system updates, regulatory filings and other activities associated with the life-cycle of a product.

Job Responsibilities:

  • Project Management Assist with projects and simple to complex technical activities associated with method improvements, method transfers, and possibly lab related activities
  • Work to meet schedules, timelines, deadlines.
  • Support staff on project teams.
  • Work with internal departments, collaborators and partners concerning projects and commitments.
  • Support coordination with customers to support multi-site operational activities.
  • Assure and apply GMP throughout operations.
  • Participate in group and project teamwork activities; project and process improvements.
  • Meets scheduled performance of 95% on time.
  • Assist in execution of projects such as method transfers, and method validations.
  • Support simple to complex technical activities associated with products, control systems, health authority filings.
  • Support methods monitoring and reference material replenishment and testing. Identify discrepancies, as applicable. ;

Skills:

  • GMP
  • Quality control
  • Quality Control
  • Method Transfers

Education/Experience:

  • BS/BA degree and minimum 2-3 years of experience in commercial quality control, preferred.
  • Education experience preferably in relevant scientific discipline and experience is in pharmaceutical or biopharmaceutical industry.
  • Knowledge of GMP quality control pharmaceutical systems strongly desired.
  • Strong skills in detailed planning with cross-functional teams
  • Ability to negotiate, influence, and make decisions in order to meet local, network, and global objectives and initiatives.
  • Strong verbal and written communication skills, ability to organize and present information both formally and informally.
  • Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in multiple analytical and/or biological test procedures.
  • Routinely exercises sound judgment, reasoning and problem solving.
  • Capable of working with moderate independence or under moderate supervision and planning priorities and supporting potentially multiple projects and teams.

Related Jobs

Biotechnologist Associate

Scientific
 New Hampshire
23.25
12 months

Location (mandatory): Portsmouth NH Looking for a candidate with science degree and some manufacturing experience

GMP
cGMP
lab work

QC Analyst I

Scientific
 California
27.93
6 months

Location (mandatory): Vacaville California With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.

laboratory testing
trend analysis
documentation review
cGMP regulations

Sr. Quality Records Investigator

Scientific
 Texas
6 months

Location (mandatory): Houston TX The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.

Deviation
investigation
capa
documentation

Medical Writer II

Scientific
Remote
12 Months (possible extension)

Location : Remote We are seeking a detail-oriented and innovative Marketing Healthcare Writer to join our team. This role focuses on creating accurate, engaging, and compliant digital content for diverse promotional channels within the healthcare sector. The ideal candidate will collaborate closely with the marketing team and leverage AI-driven tools to streamline content development while ensuring quality and compliance

MLR (Medical
Legal
Regulatory)
Digital Marketing
AI tools and content generation
Medical Writing

Validation Engineer II

Scientific
 New Hampshire
7 Months

Location : Portsmouth NH Validation Engineer II responsible for Computer System Validation (CSV) in a regulated biotech/pharma manufacturing environment, ensuring GMP compliance for automation, process control, and MES systems while supporting site and process improvement initiatives.

CSV
Deltav

US Scientist I (PO&T)

Scientific
 Massachusetts
12 Months

Location : Cambridge MA, USA 02142 The Analytical Development team is seeking a highly self-motivated analytical chemist to join us for a 12-month contract. This role will support analytical method development for small molecule and oligonucleotide programs. This position requires expertise in analytical chemistry and extensive experience in analytical techniques such as LC, LC-MS, GC, and GC-MS. The position also requires adequate knowledge of organic chemistry or pharmaceutical science. Hands-on experience with high resolution mass spectroscopy (HRMS) and prep LC would be a plus.

Method development
LC-MS
HPLC
GC-MS

Lab Technician I

Scientific
 Illinois
6 months

Location: Rockford, IL 61103 Performs a variety of laboratory tasks under the supervision of a Scientist/Researcher. The technician will use both standard procedures and adapted processes to support specific projects and routine operations, while collaborating with maintenance staff to ensure smooth equipment functioning.

Test Schedule
Supervision
Laboratory Work

Quality Assurance Associate

Scientific
 North Carolina
12 Months

Location : Sanford, NC. The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation.

Validation
Qualification
Review and approve

Contract Membership Specialist

Scientific
Remote
12 Months (possible extension)

M-F, 8am - 5pm. Full time, No OT... 100% Remote, Needed for at least one year, high possibility to extend for the full two years, No specific area/degree but must have a Bachelors Degree minimum... Candidate must be willing to participate/lead meetings and team calls occasionally. Manager values a candidate that is highly driven to learn to skills and take on new projects voluntarily. Manager likes candidates that are inquisitive. Need someone who is HIGHLY analytical. They'll be searching various systems, if they see something wrong they'll need to "go down the rabbit hole" to find out "why?" Need strong critical thinking skills to know when to search system to system for various bits of info. Must have experience working with multiple large data management systems, contracts and pricing, and/or contract development and analytics. Must have very strong writing/grammar and communication skills. Needs to have high attention to detail and accuracy. Interviews will be one with manager and then a panel interview. Must be able to perform high level Excel functions, formulas, vlook-ups. BONUS - manager would like to see Excel test scores. Resolve membership affiliation and inquiries from account management teams. Monitor Revenue Manager platform and boundary systems to confirm data accuracy. Responsibility for managing daily business tasks and processes with internal/external key stakeholders. Access and process data within reporting tools, including Revenue Manager, MicroStrategy, and boundary systems. Communicate and resolve membership discrepancies with internal and external customers; resolve inquires, maintain synchronization and integrity of membership. Create, maintain, and support a collaborative environment with external customers and internal business partners. Responsible and accountable for data compliance activities within membership and the oversight and execution of applicable processes and business decisions to achieve compliance. Ensure accurate and up-

Model N
SAP
SAP-ishift
Contracting
Pricing
Membership
logo

At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.


2025. All right reserved.
logologologologo