Find & Apply For Production Plant Manager Jobs in Paramount, California

Production (Manufacturing) and Documentation Control Manager DLC Laboratories, Inc. Paramount, CA Job Details Full-time $90,000 - $110,000 a year 4 hours ago Benefits Health insurance Vision insurance Life insurance Retirement plan Qualifications Data integrity assurance Manufacturing management Teamwork Microbiology Interpersonal skills pH meters pH sensors High-performance liquid chromatographs Digital signature usage Data management Attention to detail Ultraviolet-visible (UV-Vis) spectroscopy Chemical analysis Fourier-transform infrared (FTIR) spectroscopy Viscosity measurements FDA regulations Full Job Description Overview Based in Paramount, California, DLC Laboratories, Inc. is one of the nation's leaders in health and beauty products for the Hispanic market. Founded in 1963, the company has grown rapidly in recent years, and our expanding product range is available in chain stores (e.g. Walmart, Target, CVS, and Walgreens) and independents throughout the USA and in foreign countries. DLC Laboratories, Inc. offers competitive compensation and excellent benefits. Salary will depend on education and experience. We are seeking a dynamic and detail-oriented Production (Manufacturing) and Documentation Control Manager to manage and coordinate the activities and operations of the Production and Documentation Control department and staff. The ideal candidate will thrive in a fast-paced environment, leveraging their leadership skills and technical knowledge to optimize workflows, uphold compliance standards, and foster cross-functional collaboration. Duties Maintains document control system that allows efficient and correct access. Prepares, reviews, revises, maintains, and approves product/business documentation including but not limited to production batch records, audit reports, quality control results, reports, policies and procedures, and standard operating procedures. Issues status for raw materials, in-process products, and finished goods. Provides expiration dating for primary and secondary packaging products. Reviews, writes, and revises standard operating procedures for department. Writes and approves specifications for finished and in-process products. Ensures timely completion of quality documentation for all products/business needs. Coordinates documentation with R D, Production and Quality Control managers. Tracks and coordinates documentation change requests, from approval through implementation. Analyzes departmental processes and recommends improvements. Prioritizes and manages multiple projects within design specifications and budget restrictions. Interacts and collaborates effectively with internal and external team members to assure the needs of the company are met. Assists in project planning; provides reports and updates as required. Performs annual product reviews and annual retained sample analysis. Reviews label proofs and assists in the preparation of Drug or Dietary Supplement Facts panels. Performs other related duties as assigned by management. Qualifications Strong knowledge of pharmaceutical manufacturing processes, computer, and equipment validation, GMPs, Food Safety and product/process validation. Thorough knowledge of GMP, CFR, and factors impacting compliance. Knowledge of and ability to utilize statistics in evaluation of data. Thorough knowledge of FDA regulations. Demonstrated proficiency in supervising and motivating subordinates. Commitment to excellence and high standards Excellent written and oral communication skills Ability to work with all levels of management. Strong organizational, problem-solving, and analytical skills Ability to manage priorities and workflow. Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Proven ability to handle multiple projects and meet deadlines. Strong interpersonal skills. Demonstrated competence in reacting to and handling emergencies. Able to work collaboratively with multiple science professionals in a busy and complex environment using tact, diplomacy, and discipline. Ability to communicate professionally and effectively in person, on the phone, electronically, or through other means to individuals and groups. Experience Working knowledge of cGMPs, Quality and regulatory requirements. Must understand and review results from HPLC, GC, FTIR, UV-Vis, pH, analytical balances, viscosity, conductivity, and basic microbiology equipment. Should be able to operate pH meter, FTIR, UV-Vis, analytical balance, viscosity equipment, density/specific gravity equipment, conductivity meter, and other routine QC instruments used at the facility.

Should be proficient in:

Instrument calibration and calibration status Preventive maintenance records Equipment logbooks Analytical method SOPs Method validation/verification System suitability Reference standards Raw data review Chromatogram review Audit trails Electronic records ALCOA+ data-integrity principles OOS investigations OOT/trending Deviations CAPA Change control Laboratory investigations Equipment qualification:

IQ/OQ/PQ

Computer Skills:

Advanced proficiency in Microsoft Office, particularly Excel and Word, with experience using ERP/MRP systems, and electronic document management systems in a regulated manufacturing environment. Strong ability to prepare and maintain production records, SOPs, batch documentation, reports, spreadsheets, and document-control records. Knowledge of electronic records, version control, audit trails, electronic signatures, and GMP data-integrity requirements is required. Education Ph.D./M.S. in related field and minimum of two years related experience or B.S. in related field and minimum of six years related experience.

Pay:

$90,000.00 - $110,000.00 per year

Benefits:

Health insurance Life insurance Retirement plan Vision insurance

Work Location:

In person