Qc Microbiology Assoc I Jobs in California

• Identify and implement manufacturing procedures intended to optimize existing processes and ensure compliance with regulatory requirements.

• Experience in flow assays a MUST

• Experience in bioassays is a plus

Introductory Experience in the use of scientific laboratory techniques, equipment and materials:

• Excellent documentation and communication skills.

• Consistent, dependable, and accurate in carrying out responsibilities

Proven history of working in a fast-paced team environment, time management, and meet deadlines.

Perform routine cleaning, schedule equipment preventative maintenance, and organization of laboratory areas in accordance with cGMP requirements

Bachelor’s Degree in chemistry, biology, or microbiology with 0-3+ years’ relevant microbiology laboratory experience in Pharmaceutical/Biotech.

Excellent knowledge of Aseptic technique and common microbiological testing

Knowledge of relevant, compliance and guidance documents

Interpersonal skills and ability to contribute to the success of a team

Solid AP for studio show, solid AD for live game coverage in PCR, PD Room and remote environments.

Operates with mastery in the digital environment, maximizing server capabilities and utilizing q-cut systems.

Thorough knowledge of current television production technologies and applies knowledge to produce compelling content.

Minimum 2 years practical production experience.

Highly strong bilingual Spanish/English speaking/writing skills.

Strong organizational and communication skills.

Detailed knowledge of quality management systems, current Good Manufacturing Practices, longstanding expertise and practice with QC principles.

Manage the creation, review and approval of technical and/or validation reports.

Perform other responsibilities as deemed necessary.

Excellent documentation, written and verbal communication skills are essential.

Coordinate troubleshooting efforts of instrumentation or reagents through hypothesis testing, laboratory notebook studies and communication with vendor technical support.

Support tracking of contract lab tests and review of data from these labs.

Strong leadership, organizational and time management skills.

Knowledge of quality systems including exception management, change control, document control, etc.

Develop and manage the performance/talent of direct reports.

Operate and troubleshoot procedures for lab equipment, and quality and regulatory requirements pertinent to pharmaceutical and combination drug manufacturing labs.

Prioritize multiple projects/workflows and manage time efficiently to meet established timelines.

Serve as a backup for QC Manager in handling Quality and Regulatory Inspections.