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Assist senior level personnel in sterile filling of a multitude of solutions including drug product, media, buffers, using an automated filling and closing machine, gowned in accordance with Class C (ISO 7) conditions. Assist senior level personnel in bulk drug formulation using a variety of lab equipment including mixers, balances, pH meters, etc., gowned in accordance with Class C (ISO 7) conditions.

HOUR

<div class="elementor-element elementor-element-af24ec0 elementor-widget elementor-widget-theme-post-content"><div class="elementor-widget-container"><div class="elementor-element elementor-element-01097f7 elementor-widget elementor-widget-heading"><div class="elementor-widget-container">Corporate Overview</div></div><div class="elementor-element elementor-element-13022a4 elementor-widget elementor-widget-text-editor"><div class="elementor-widget-container"> <div class="elementor-text-editor elementor-clearfix">Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides the quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.</div></div></div></div> <div class="elementor-widget-container">Pay Range</div> <div class="elementor-widget-container">The pay range for this position is $22.00 - $24.00 per hour. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications.</div> <div class="elementor-widget-container">Position Overview</div><div class="elementor-widget-container">This is a temporary-to-hire, on-site position supporting bulk formulation and/or filling operations for sterile liquid injectable pharmaceutical products under cGMP regulations. The role is Monday-Friday, 8 hours/day (excluding lunch) with a flexible start between 7:00-9:00 am. Overtime, weekends, and holidays may be required.</div><div class="elementor-widget-container">Duties and Responsibilities <ul><li>Perform various routine manufacturing tasks under the direction of internal SOP's and cGMP guidelines</li><li>Prepare material components for manufacturing operations</li><li>Document steps clearly and completely in production batch records, logbooks and other controlled forms</li><li>Participate in inspection readiness activities</li><li>Perform basic arithmetic and algebraic computation</li><li>Maintain cleanliness of areas and equipment</li><li>Assist senior level personnel in bulk drug formulation using a variety of lab equipment including mixers, balances, pH meters, etc., gowned in accordance with Class C (ISO 7) conditions</li><li>Assist senior level personnel in sterile filtration activities, gowned in accordance with Class C (ISO 7) conditions</li><li>Assist senior level personnel in sterile filling of a multitude of solutions including drug product, media, buffers, using an automated filling and closing machine, gowned in accordance with Class C (ISO 7) conditions</li><li>Collect and dispose of lab wastes according to established procedures</li><li>Collaborate in continuous improvement activities</li><li>This position may require local travel between company facilities within a short distance (approximately 3 miles) based on business needs.</li></ul>Education and Experience Requirements<ul><li>High school diploma or equivalent with 1 - 2 years relevant experience is required, a Bachelor's in an Engineering discipline or Life Science field preferred</li><li>Time and project management skills with the ability to multi-task are essential</li><li>Must be able to effectively communicate within department and cross-functionally with other divisions</li><li>High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction</li><li>Experience in a growth-oriented, cGMP contract manufacturing organization with a focus on compliant execution of business, is a plus</li></ul></div></div><div class="elementor-element elementor-element-01097f7 elementor-widget elementor-widget-heading">Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies with all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.</div>

Argonaut Manufacturing Services

Drug Product Manufacturing Associate I

Biology

Biotech and Pharmaceutical

Communication Skills

Continuous Improvement

Contract Manufacturing

Cross-Functional

Current Good Manufacturing Practice (cGMP)

Drug Manufacturing

Drug Products

High School Diploma

ISO (International Organization for Standardization)

Laboratory Equipment

Manufacturing

Manufacturing Operations

Multitasking

On Site Support

Project/Program Management

Regulations

Standard Operating Procedures (SOP)

State Laws and Regulations

Supply Chain

Time Management

Travel Industry

Willing to Travel

Talent Acquisition

Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with 2+ years of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field with 3+ years of related experience; or High school diploma/equivalent with 5+ years of related manufacturing experience in a cGMP environment. Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with at least 1 year of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field; or High school diploma/equivalent with 3+ years of related manufacturing experience in a cGMP environment.

Corporate OverviewArgonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.Benefits and Pay RangePay range for this position is $21.00 - $27.00 per hour, depending on experience. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. This is a temp to hire position.Position OverviewThe Manufacturing Technician II/III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides.This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Start time for this position is 12:00 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance.Responsibilities and Duties<ul><li>Ability to work within an ISO 13485 and cGMP production environment and ensure compliance with our quality system.</li><li>Execute documentation based on cGMP and GDP procedures, as well as perform documentation review post manufacturing execution.</li><li>Participate in Quality Working Teams and Continuous Improvement Teams.</li><li>Visual inspection of lyophilized product and heat seals of packaging. </li><li>Clean and sanitize manufacturing and associated support areas.</li><li>Responsible for monitoring machinery and reporting alarms to lead technician or Supervisor. </li><li>Conduct daily documentation review.</li><li>Participate in Quality Working Teams and Continuous Improvement Teams.</li><li>Operate large machinery and monitor automated.</li><li>Employee may be required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. </li><li>Perform daily arithmetic calculations as it pertains to total volume and liquid concentrations. </li><li>Perform daily unit conversions as it pertains to gravimetric and volumetric measurements.</li><li>Operate production equipment such as pipettes, balances, pH meter and heat sealers.</li><li>Monitor department equipment for proper operation that is within calibration.</li><li>May perform safety and cGMP inspections or observations. </li><li>Ensure compliance with SOP/cGMP and cGDP requirements. </li><li>Assist in training/ leading of new team members in production activities.</li><li>Assist in updating and new revision of standard operating procedures (SOP).</li><li>May need to be an author for any MFG Non-Conformance Reports (NCR) and risk analysis memos.</li><li>Receive and distribute supplies into the production area as necessary. </li><li>Perform NetSuite transaction, issue material, completion and closing of work orders.</li><li>This position may require local travel between company facilities within a short distance (approximately 3 miles) based on business needs.</li><li>May assist with review of quality assurance logbooks.</li><li>May perform other duties as assigned.</li></ul>Education RequirementsLevel II<ul><li>Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with at least 1 year of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field; or High school diploma/equivalent with 3+ years of related manufacturing experience in a cGMP environment.</li></ul>Level III<ul><li>Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with 2+ years of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field with 3+ years of related experience; or High school diploma/equivalent with 5+ years of related manufacturing experience in a cGMP environment.</li></ul>Required Skills and Knowledge<ul><li>Punctuality and reliable attendance required.</li><li>Ability to read and follow detailed written instructions; strong verbal and written communication skills.</li><li>Proficient in reading, writing, and conversing in English to understand cGMP manufacturing processes and SOPs.</li><li>Knowledge of manufacturing production processes related to product integrity, including visual inspection of components and finished goods, manual and semi-automated packaging, and product labeling.</li><li>Understanding of basic chemical and biological safety procedures.</li><li>Basic knowledge of formulation, filling, and kitting operations and capabilities.</li></ul>Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.

Manufacturing Technician II or III

Biochemistry

Calibration

Corporate Compliance

Documentation

Documentation Review

English Language

Environmental Health

Geography

Hazardous Materials/Substances

Mail Processing

Maintain Compliance

Manufacturing/Industrial Processes

Molecular Biology

NetSuite

Presentation/Verbal Skills

Production Systems

Quality Assurance

Safety Process

Safety/Work Safety

Team Lead/Manager

Writing Skills

Performs sterile filling of a multitude of solutions including drug product, media, buffers, using an automated filling and closing machine, gowned in accordance with Class C (ISO 7) conditions. Performs bulk drug formulation using a variety of lab equipment including mixers, balances, pH meters, etc., gowned in accordance with Class C (ISO 7) conditions .

Corporate OverviewArgonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides the quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.Pay Range The pay range for this position is $24.00 - $28.00 per hour. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications.Position and ScopeThis is a temporary-to-hire, on-site position supporting bulk formulation and/or filling operations for sterile liquid injectable pharmaceutical products under cGMP regulations. The role is Monday-Friday, 8 hours/day (excluding lunch) with a flexible start between 7:00-9:00 am. Overtime, weekends, and holidays may be required.Duties and Responsibilities<ul><li> Performs various routine manufacturing tasks under the direction of internal SOP's and cGMP guidelines.</li><li> Prepares material components for manufacturing operations</li><li> Documents steps clearly and completely in production batch records, logbooks and other controlled forms </li><li> Participates in inspection readiness activities.</li><li> Performs basic arithmetic and algebraic computation </li><li> Maintain cleanliness of areas and equipment</li><li> Performs bulk drug formulation using a variety of lab equipment including mixers, balances, pH meters, etc., gowned in accordance with Class C (ISO 7) conditions </li><li> Performs sterile filtration activities, gowned in accordance with Class C (ISO 7) conditions</li><li> Performs sterile filling of a multitude of solutions including drug product, media, buffers, using an automated filling and closing machine, gowned in accordance with Class C (ISO 7) conditions</li><li> Participates in the execution of validations/qualifications of new processes and equipment </li><li> Collects and disposes of lab wastes according to established procedures </li><li> Collaborate in continuous improvement activities</li><li>This position may require local travel between company facilities within a short distance (approximately 3 miles) based on business needs.</li></ul><h3>Education and Experience Requirements</h3><ul><li> High School Diploma or Equivalent with 2 - 4 years relevant experience is required, a Bachelors in an Engineering Discipline or Life Science Field preferred. </li><li> Time and project management skills with the ability to multi-task are essential.</li><li> Must be able to effectively communicate within department and cross functionally with other divisions. </li><li> High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction.</li><li> Experience in a growth-oriented, cGMP contract manufacturing organization with a focus on compliant execution of business is a plus.</li></ul>Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.

Drug Product Manufacturing Associate II

The purpose of this position is to participate in tasks related to the visual inspection of manufactured liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing as well as other types of visual inspection activities, as required. Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations.

Corporate OverviewArgonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.Pay Range The pay range for this position is $20.00 - $22.00 per hour. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications.Position OverviewThe purpose of this position is to participate in tasks related to the visual inspection of manufactured liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing as well as other types of visual inspection activities, as required.This role is 100% on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 6:00 am - 9:30 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance.Responsibilities and Duties<ul><li>Perform visual inspection of pharmaceutical or medical products to identify defects or non-conformities.</li><li>Ensure all inspected products meet established quality standards and regulatory requirements.</li><li>Document results accurately in batch records or electronic systems.</li><li>Maintain good documentation practices (GDP) and ensure inspection areas comply with aseptic and cleanliness standards.</li><li>Operate and maintain inspection equipment and booths according to SOPs.</li><li>Report defective products or process deviations to quality or production supervisors.</li><li>Follow Good Manufacturing Practices (GMP) and safety protocols at all times.</li><li>Participate in inspection and manufacturing readiness activities.</li><li>Maintain cleanliness and organization of inspection areas, including gowning in all lab areas.</li><li>This position may require local travel between company facilities within a short distance (approximately 3 miles) based on business needs.</li></ul>Requirements and Qualifications<ul><li>High school diploma or equivalent required; 0-2 years of relevant experience. A Bachelor's degree in an engineering discipline or life science field is preferred.</li><li>Must be able to effectively communicate within department and cross functionally with other divisions. </li><li>High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction.</li><li>Familiarity with GMP guidelines, including USP<790> and USP<1790>, and 21CFR 210/211</li><li>Proficiency in Microsoft Office; including Word, Excel, and Overlook</li></ul>Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.

Visual Inspection Technician

Code of Federal Regulations

Debugging Skills

Equipment Maintenance/Repair

GMP (Good Manufacturing Practices)

Medical Products

Microsoft Excel

Microsoft Word

Production Management

Quality Management

Quality Metrics

Regulatory Requirements

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Drug Product Manufacturing Associate IArgonaut Manufacturing Services

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Visual Inspection TechnicianArgonaut Manufacturing Services

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