Bulk Formulation Chemist I

table.MiTabla { max-width: 1020px;!important Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Summary: Grifols Diagnostics Solutions is seeking a Bulk Formulation Chemist I in San Diego, CA. This position is responsible for the manufacture of bulk clinical and commercial kit reagents. Responsible for sub-assembly formulation, raw material prep and/or processing, QC testing reagent or component formulation and some in-process testing. Participate in transfer, support activities and continuous improvement on existing processes. May be assigned to one or more functional Manufacturing areas. In order to be successful in this position, we are looking for at least a Bachelors Degree in Microbiology, Biology, Chemistry, Chemical Engineering or related field. Primary responsibilities for role: Responsible for the staging of raw material and formulation of reagent bulks or constituents. Maintains, measures and dispenses materials. Performs material and labor transactions in the Enterprise Resource Planning (ERP) System. Understands and executes written procedures in accordance with cGMP. Maintains detailed and accurate device history records with cGMP. Completes and forwards device history records for review in a timely manner. General manufacturing area housekeeping including cleaning of labware, equipment, shelves, benches and sinks and removing trash. Ensures proper transportation, handling, and disposal of hazardous, bio-hazardous and/or infectious substances. Operates and calibrates as needed all general lab equipment. Follows all safety rules. Maintains accurate and complete training records. Maintains and archives Manufacturing log sheet records. Must be able to communicate product issues, safety incidences and/or personal issues affecting production timelines. Performs regular cycle count activities to maintain inventory accuracy. May be working on processes and observed during audits, including ISO, FDA and internal audits. Participates in continuous improvement projects. Additional Responsibilities: Cross-functional communication participation. Assists fill crew as needed. Responsible for flushing water ports and eyewash stations. Adhere to target manufacturing timelines. Attentiveness and openness to learn new processes. Maintains implemented 5S. Knowledge, Skills, and Abilities: Demonstrated job specific technical knowledge. Working knowledge of Microbiology, Biology, or Chemistry. Working knowledge of laboratory safety and record keeping. Blood Borne Pathogen Training. Basic to intermediate knowledge in the operation of analytical balances, pipettes, filter integrity testers, peristaltic pumps, water baths and spectrophotometers. Basic to intermediate-level knowledge on the operation of complex laboratory equipment and processes. Working knowledge of Microsoft Office software. Attention to detail and ability maintain accurate inventory accounts, good organizational skills and team oriented. Ability to follow oral and written instructions Education: Typically requires High school Diploma or Associate's (AA) degree in Microbiology, Biology, Chemistry, Chemical Engineering or related field. Experience: 0+ to 2 years of related experience in a laboratory setting with an Associate’s degree 2 to 4 years’ experience in a laboratory or commercial manufacturing setting with a High School Diploma. At least 1 year of experience with Good Documentation Practices (GDP), Current Good Manufacturing Practices (cGMP) and ISO 13485 Regulations is highly preferred Equivalency: Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor’s degree. Occupational Demands: The physical demands are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Visually inspect components and final kits for compliance and specifications. Close vision (20 inches or less) will be utilized and some color identification will be required. Frequently required to perform reaching, bending, stooping or kneeling motions. Operators may be required to walk and stand for a considerable amount of time. Operators frequently use hands/fingers to handle or feel, open tightly sealed containers/tanks, and utilize hand tools. Operator will occasionally climb step stools/ladders as needed. May frequently or continuously lift, carry, push, pull or otherwise manipulate objects up to 10 pounds in weight. May occasionally lift, carry, push, pull or otherwise manipulate objects up to 50 pounds in weight. May move heavier (greater than 50lbs) objects and/or materials using carts or pallet jacks.

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The estimated pay scale for Bulk Formulation Chemist I role based in San Diego, California, is $24.02 to 30.03 per hour Additionally, the position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us! Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. California Personnel Privacy Policy and Notice at Collection Location: NORTH AMERICA : USA : CA-San Diego:USSDW - San Diego CA - Willow Ct Mfg Learn more about Grifols