Energy Jobline ZR
Operations Technical Specialist 1 in San Diego
Energy Jobline ZR, San Diego, California, United States, 92189
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Duration: 06 months
Shift: 1st Shift
Pay Rate: $26.00 - $30.00/hr
Job Summary
The Operations Technical Specialist 1 supports various areas of manufacturing including production and testing by, under guidance, executing tasks for resolution of technical challenges, business continuity or continuous improvement initiatives related to product or processes. Essential Duties and Responsibilities
The incumbent may be asked to perform other function‑related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Primary responsibility for this position is supporting scientific staff with experiments or other activities for resolution of challenges related to release of product such as nonconformance investigations. Under guidance, execute protocols as well as generate data summaries using data analysis tools. Occasionally may be responsible for performing testing for GMP release of product. Operates laboratory equipment to generate timely, reliable, and accurate data. Performs activities essential to laboratory daily operations (e.g., equipment maintenance, executing cleaning requirements, upkeep of supplies, etc.). Maintains a working knowledge of Hologic assays, technology, and instrumentation. Performs tasks to support efforts related to resolution of quality records, technical challenges, business continuity or continuous improvement efforts. Physical Demands
Sit; use hands to finger, handle or feel objects, tools, or controls. Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl. Lifting/moving and carrying products weighing up to 40 pounds. Exposure to moving mechanical parts, vibration and/or moderate noise levels. Exposure to hazardous chemicals or other materials. Safety Shoes with Impact and Compression Protection Must be worn. Exposure to blood. Education
BA or BS degree and 1-3 years related experience in scientific discipline. Experience
Knowledge of cGMP, QSR and ISO regulated environments including knowledge of compliance enforcement necessary for 510K and PMA products. Skills
Conducts tasks in accordance with Good Laboratory Practices (GLP). Ability to operate and perform limited trouble shooting of complex lab equipment. Demonstrates strong peer to peer communication skills as well as possessing the ability to effectively communicate inter‑departmentally. Ability to analytically interpret data of minor complexity and present to peers. Ability to triage tasks with competing priority and recognize sense of urgency. Willingness and ability to adhere to FDA cGMP, ISO13485, company and department procedures. Ability to work well under supervision and take direction on increasingly complex projects. Working knowledge of scientific writing techniques. Affinity for a workload focused on laboratory centered tasks. Ability to execute tasks in line with productivity expectations. Must follow all applicable FDA regulations and ISO requirements. Company Description
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top‑tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best‑in‑business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier awards, further validating our industry‑leading capabilities. If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
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The Operations Technical Specialist 1 supports various areas of manufacturing including production and testing by, under guidance, executing tasks for resolution of technical challenges, business continuity or continuous improvement initiatives related to product or processes. Essential Duties and Responsibilities
The incumbent may be asked to perform other function‑related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Primary responsibility for this position is supporting scientific staff with experiments or other activities for resolution of challenges related to release of product such as nonconformance investigations. Under guidance, execute protocols as well as generate data summaries using data analysis tools. Occasionally may be responsible for performing testing for GMP release of product. Operates laboratory equipment to generate timely, reliable, and accurate data. Performs activities essential to laboratory daily operations (e.g., equipment maintenance, executing cleaning requirements, upkeep of supplies, etc.). Maintains a working knowledge of Hologic assays, technology, and instrumentation. Performs tasks to support efforts related to resolution of quality records, technical challenges, business continuity or continuous improvement efforts. Physical Demands
Sit; use hands to finger, handle or feel objects, tools, or controls. Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl. Lifting/moving and carrying products weighing up to 40 pounds. Exposure to moving mechanical parts, vibration and/or moderate noise levels. Exposure to hazardous chemicals or other materials. Safety Shoes with Impact and Compression Protection Must be worn. Exposure to blood. Education
BA or BS degree and 1-3 years related experience in scientific discipline. Experience
Knowledge of cGMP, QSR and ISO regulated environments including knowledge of compliance enforcement necessary for 510K and PMA products. Skills
Conducts tasks in accordance with Good Laboratory Practices (GLP). Ability to operate and perform limited trouble shooting of complex lab equipment. Demonstrates strong peer to peer communication skills as well as possessing the ability to effectively communicate inter‑departmentally. Ability to analytically interpret data of minor complexity and present to peers. Ability to triage tasks with competing priority and recognize sense of urgency. Willingness and ability to adhere to FDA cGMP, ISO13485, company and department procedures. Ability to work well under supervision and take direction on increasingly complex projects. Working knowledge of scientific writing techniques. Affinity for a workload focused on laboratory centered tasks. Ability to execute tasks in line with productivity expectations. Must follow all applicable FDA regulations and ISO requirements. Company Description
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top‑tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best‑in‑business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier awards, further validating our industry‑leading capabilities. If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
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