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Weekend Biotech Quality Control Jobs in New York

QC Chemist

Central Islip, NY · On-site

$65K - $90K/wk

Job Title: QC Chemist I Location: Central Islip, NY (Onsite) Job Type: Full-Time | Permanent Shift ... Must be willing to work weekday shifts and occasional weekends depending on business needs. * Must ...

Quality Control Coordinator

Manhattan, NY · On-site

$21.75 - $30/hr

Position Purpose/Summary The Quality Control Coordinator is committed to supporting Louisiana ... weekends, and/or holidays, as needed, to best serve the business operations. Benefits Acciona ...

Quality Control Coordinator

Manhattan, NY · On-site

$21.75 - $30/hr

Position Purpose/Summary The Quality Control Coordinator is committed to supporting Louisiana ... weekends, and/or holidays, as needed, to best serve the business operations. Benefits Acciona ...

Quality Control Raw Material Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

... biotech, or CDMO/IDMO environment, with direct experience in raw material or incoming quality control functions preferred * Working knowledge of USP compendial methods relevant to raw material ...

Quality Control Analyst

Summit, NJ

$25.50 - $34.25/hr

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and ...

Quality Control Tech

Newark, NJ · On-site

$24.36 - $28.52/hr

Arcosa Asphalt is seeking a Quality Control Technician based out of our Asphalt locations ... May require overtime and weekends * Other duties or responsibilities as assigned About You * Prompt ...

BSc in Chemistry, Biology, Pharmacy, Biotechnology, Biomedical Engineering, or related experience. Advanced Degree is preferred. * 10+ years' experience in Quality Control, Quality Assurance, Quality ...

Quality Control Tech

Newark, NJ · On-site

$24.36 - $28.52/hr

Arcosa Asphalt is seeking a Quality Control Technician based out of our Asphalt locations ... May require overtime and weekends * Other duties or responsibilities as assigned About You * Prompt ...

Showing results 21-40

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Infographic showing various Weekend Biotech Quality Control job openings in New York as of August 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 100% In-person job distribution.

Quality Control Microbiology Supervisor

Lynkx Staffing LLC

Saddle Brook, NJ • On-site

Full-time

Re-posted 23 days ago


Job description

Quality Control Microbiology SupervisorAllendale, NJ The Quality Control Microbiology Supervisor organizes, and directs staff to meet and exceed cGMP requirements, establish KPI’s, while adhering to quality control-microbiological and technical standards. Provides oversight of day to day activities including adjustment of workflow, test performance, and quality compliance.
  • Team Leadership - Interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems for the following positions. Directly supervised the following roles: QC Microbiology Associates
  • Investigate and document non-confirming events and environmental excursions.
  • Troubleshoot and recommend process improvements to achieve greater efficiency ad meet quality goals.
  • Interact with other Microbiology departments on a regularly scheduled basis to discuss and harmonize best practices, procedures and processes between the sites.
  • Participate in department and cross functional meetings.
  • Ensure compliance with regulatory agency requirements by enforcing a quality culture throughout the department.
  • Interact with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns.
  • Author and revise Standard Operating Procedures, Work Instructions, forms and Protocols to reflect current practices.
  • Perform microbiological and environmental monitoring data review. Compile and issue quarterly and annual Environmental Monitoring trending reports.
  • Provide staff development through feedback aimed towards performance development and review.
  • Ability to remain focused and effective in high stress situations.
  • Builds constructive working relationships characterized by a high level of acceptance, cooperation, and mutual respect.
  • Able to handle challenging interpersonal relationships.
  • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
  • Aseptic Processing Standards
REQUIREMENTS
  • BS in Microbiology or relevant field required.
  • Biotechnology Certificate and/or cGMP experience
  • Minimum of 3 years of experience with environmental monitoring or within the biopharmaceutical industry.
  • Strong knowledge of microbiological test methods, philosophies, method validation and method transfer.
  • Strong knowledge of quality systems and ability to interpret Quality standards of implementation and review.
  • Proficient with computer software with MS Office, Excel, and MODA.
  • Must have ability to work in a team-oriented environment and with vendors.
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen
  • Must have the ability to work in the cleanroom environment for extended period of time
  • Must have the ability to work with specialized equipment
  • Must be able to handle the standard/moderate noise of the manufacturing facility
  • The employee must be able to comply with personal hygiene standards as they apply to aseptic processing. The employee must successfully complete sterile gowning training/qualification and aseptic process qualification (personal media fill) as well as annual/semiannual re-qualification as a core competency requirement of their employment in this role.
  • An individual may exert up to 10 pounds of force occasionally or a negligible amount of force frequently to lift, carry, push, pull, or otherwise move objects.
  • Must be physically capable to stand, walk, sit, bend, stretch, use hands to handle or feel, reach with hands and arms, and talk or hear.
  • The employee is frequently required to lift and/or move up to 30 pounds and occasionally move tanks up to 300 pounds (with assistance)
  • Heavy cryo-gloves must be used when working with liquid nitrogen
  • While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noise.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.