Summary
Overview
Work History
Education
Skills
Certification
Training
Timeline
Generic

Samuel Springs

Bloomington,IN

Summary

I have more than twelve years of QC experience working in quality. I also have a proven track record for building some of the best teams onsite. To further complement my experience, I have more than eight years of experience in method development, instrumentation setup, validation, and qualification.

Overview

9
9
years of professional experience
1
1
Certification

Work History

QC Chemistry Supervisor

Catalent
08.2023 - 03.2024
  • Follow and adhere to the strict safety culture and practices
  • Reduce Invalids by 80% in the first three months
  • Increased Right First Time 65-75% to 98% for most analyst in one quarter
  • Authored project for overall positive trend for QC Chemistry metrics
  • Lead Drug Substance project which resulted in 6
  • Responsible for 6 direct reports, performance, and career development
  • Periodic 1:1s to establish working relationships, develop careers, and offer support and guidance to reports
  • Responsible for daily communication with customers and potential customers
  • Work in collaboration with senior management to adhere to budget and department finances
  • Manage and oversee all Quality Control testing on in-process and final products
  • Lead on 5S Project for area and group
  • Maintain a clean and safe work environment
  • Follow cGMP guidelines and other quality standards
  • Ensure that reports adhere to safety and GMP guidelines daily while performing tasks
  • Initiate OOS’s, OOT’s and deviation investigations and reporting.
  • Implemented Lean Six Sigma methodologies to optimize laboratory processes, resulting in reduced turnaround times for analyses.
  • Established effective communication channels between departments for enhanced collaboration on interdisciplinary projects.
  • Conducted routine calibration of instrumentation to maintain accurate measurements and data integrity.
  • Streamlined laboratory processes for increased efficiency and productivity by optimizing workflows.
  • Promoted a culture of teamwork among staff members while maintaining individual accountability for achieving personal performance metrics.
  • Enhanced lab safety by implementing and enforcing strict chemical handling procedures.
  • Evaluated vendor proposals, selecting those that aligned with company goals for cost-effectiveness and quality assurance.
  • Maintained high-quality standards with thorough analysis and documentation of test results.
  • Reduced waste generation through efficient use of resources, contributing to environmental sustainability efforts.
  • Actively participated in regulatory compliance audits, demonstrating adherence to established guidelines and protocols.
  • Coordinated with external partners such as contract labs or suppliers to ensure seamless collaboration on projects.
  • Utilized statistical techniques for data interpretation, facilitating informed decision-making based on empirical evidence.
  • Led continuous improvement initiatives within the chemistry department, resulting in cost savings and process enhancements.
  • Managed inventory of chemicals and equipment, ensuring proper storage and disposal practices were followed.
  • Analyzed and interpreted laboratory data.

QC Biochemistry Supervisor (Nights)

Lonza Pharmaceuticals
04.2022 - 07.2023
  • Follow and adhere to strict safety culture and practices
  • Responsible for 8 direct reports, performance, and career development
  • Increased On Time Delivery from 70% to roughly 90% over two quarters
  • Established readiness program to support and develop team to meet tight deadlines for new product introductions
  • Periodic 1:1s to establish working relationships, and career development, and offer support and guidance to reports
  • Manage and oversee all Quality Control testing on in-process and final products
  • Maintain clean and safe work environment
  • Follow cGMP guidelines and other quality standards
  • Ensure that reports adhere to safety and GMP guidelines daily while performing tasks
  • Coordinates and communicates delays and technical issues to management promptly
  • Ensure compliance with current compendia
  • Reports discrepancies and nonconforming materials to management and supports subsequent investigations; initiates and monitors progress of raw material and analytical Quality event records (e.g., deviations and CAPAs) and conducts investigations to determine root cause and possible resolution.
  • Oversaw daily operations of the department, ensuring smooth workflow and timely completion of tasks.
  • Applied strong leadership talents and problem-solving skills to maintain team efficiency and organize workflows.
  • Handled customer complaints, resolved issues, and adjusted policies to meet changing needs.
  • Monitored workflow to improve employee time management and increase productivity.
  • Improved customer satisfaction with timely response to inquiries, addressing concerns, and finding effective solutions.
  • Maintained compliance with company policies, objectives, and communication goals.
  • Evaluated employee performance and coached and trained to improve weak areas.
  • Increased team productivity by implementing efficient workflows and setting clear expectations for staff members.
  • Mentored newly hired employees on operating equipment and safety and developed training manual to use for reference.
  • Resolved conflicts among team members promptly, maintaining a harmonious working environment conducive to productivity.
  • Enhanced communication within the team by holding regular meetings and encouraging open dialogue among all members.
  • Maintained clean and well-organized production areas to avoid violations or unnecessary work delays due to hazards or inefficient layouts.
  • Demonstrated commitment to the organization''s core values, leading by example and fostering a culture of excellence.
  • Collaborated with other departments to achieve organizational goals, fostering teamwork across various functions.
  • Enforced rules and regulations outlined in company manual to set forth expectations comprehensibly and consistently.
  • Mentored junior staff members in their career development, sharing knowledge from years of experience in the field.
  • Conducted performance evaluations for staff members, identifying areas of improvement and guiding professional development plans.
  • Reduced employee turnover by fostering a positive work environment and providing ongoing feedback to staff members.
  • Identified unsafe or unhealthful workplace conditions or hazards to enforce safe work practices and procedures.
  • Developed staff skills through targeted training programs, resulting in improved performance and career growth opportunities.
  • Established performance metrics for the team, consistently tracking progress towards goals and making adjustments as needed.
  • Identified operational inefficiencies and implemented corrective measures, leading to an overall increase in effectiveness.
  • Streamlined operations for increased efficiency through regular process reviews and implementing necessary changes.
  • Solicited customer feedback to identify and improve on areas of weakness.
  • Cultivated strong relationships with key clients or stakeholders through consistent communication and excellent service delivery.
  • Led major initiatives within the department that drove innovation or addressed critical business challenges.
  • Evaluated staff performance and provided coaching to address inefficiencies.

Supervisor, Chemistry

Alcami Corporation
04.2021 - 04.2022
  • Follow and adhere to the strict safety culture and practices
  • Responsible for 6 direct reports, performance, and career development
  • Responsible for daily communication with customers and potential customers
  • Communicated frequently with customers to resolve any customer-related complaints or issues
  • Work with senior management to adhere to budget and department finances
  • Manage and oversee all Quality Control testing on raw materials, API, finished products, and excipient
  • Maintain a clean and safe work environment
  • Follow cGMP guidelines and other quality standards
  • Ensure that reports adhere to safety and GMP guidelines daily while performing tasks
  • Coordinates and communicates delays and technical issues to management promptly
  • Perform compendial reviews related to USP/NF, EP, etc.
  • Applied strong leadership talents and problem-solving skills to maintain team efficiency and organize workflows.
  • Monitored workflow to improve employee time management and increase productivity.
  • Improved customer satisfaction with timely response to inquiries, addressing concerns, and finding effective solutions.
  • Devised and implemented processes and procedures to streamline operations.

QC Lab Supervisor API

Ani Pharmaceutical Inc
12.2019 - 04.2021
  • Follow and adhere to strict safety culture and practices
  • Responsible for managing and directing 9 direct reports which included chemists and lab techs
  • Execute Quality Control testing on raw materials, API, and excipients
  • Maintain clean and safe work environment
  • Follow cGMP guidelines and other quality standards
  • Ensure that reports adhere to safety and GMP guidelines daily while performing tasks
  • Reviewed compendial reviews related to USP/NF, EP, etc
  • Review test procedures, tech transfers, and validation protocols
  • Ensure compliance with current compendia
  • Responsible for updating AD, PD, and regulatory of compendial changes and updates
  • Maintain and perform performance reviews of the team to support laboratory objectives
  • Manage and review all calibrations and preventive maintenance for instruments in the QC lab
  • Monitors and evaluates current testing processes, making recommendations for improvements when necessary
  • Also identifies and responds to out-of-trend RM results and participates in out-of-trend and out-of-specification investigations
  • Good problem-solving skills/analytical troubleshooting.
  • Maintained a safe and efficient laboratory environment by enforcing strict adherence to safety protocols and guidelines.
  • Assisted in budget management by monitoring expenses and identifying cost-saving opportunities within the lab operations.
  • Developed training materials and conducted workshops to enhance staff knowledge in specific areas of expertise.
  • Contributed to the continuous improvement initiatives within the department, promoting a culture of innovation and excellence.
  • Managed inventory of laboratory supplies, reducing waste while maintaining adequate stock levels for smooth operations.
  • Reduced turnaround time for test results by optimizing workflows and equipment usage.
  • Improved lab efficiency by implementing streamlined processes and procedures.
  • Conducted employee performance evaluations regularly, offering constructive feedback to promote growth.
  • Collaborated with other departments to improve overall patient care and diagnostic services.
  • Increased productivity by effectively scheduling staff shifts, balancing workloads, and assigning appropriate tasks based on individual strengths.
  • Enhanced the accuracy of test results through meticulous quality control measures.
  • Participated in interdepartmental meetings to ensure open communication between teams, fostering a collaborative work environment.
  • Coordinated with external vendors for supply purchases or service requests as necessary.
  • Oversaw equipment maintenance schedules, minimizing downtime due to malfunctions or repairs.
  • Led a team of laboratory technicians, ensuring high-quality performance and professional development.
  • Evaluated new technologies and methodologies for potential integration into existing lab processes, enhancing capabilities and services offered.
  • Ensured compliance with regulatory standards by conducting regular audits and updating policies as needed.
  • Provided technical guidance and support for complex testing procedures, improving overall staff competency.
  • Monitored testing procedures to meet criteria and maintain quality control.
  • Maintained safe, tidy and organized laboratory environment for accurate test results.
  • Maintained documentation on tests performed in lab.
  • Tracked collected specimens by initialing, dating, and noting times of collection.
  • Performed testing and quality control using approved laboratory procedures and instrumentation.
  • Inspected laboratory equipment to maintain good working condition for optimal results.
  • Collaborated with other departments to establish cohesive laboratory operations.

QC Laboratory Supervisor

Oxiteno USA LLC
12.2014 - 02.2019
  • Manage and direct lab techs and other chemists on methods
  • Managed and oversaw 8 direct reports which included chemists and lab techs
  • Responsible for maintaining the laboratory budget to support the financial goals of the organization
  • Encouraged collaboration between budget management teams and executive leadership to develop financial plans to support company strategic initiatives
  • Provide technical input and guidance to ensure the quality of testing
  • Support laboratory processes, process improvement, and troubleshooting
  • Set up new instrumentation and method development for new product introduction while collaborating with other teams
  • Constantly seeking out new opportunities for improved processes and cost reduction
  • Establish HPLC and GC methods and train staff in new methods
  • Help participate in the validation of methods
  • Proficient in the use of HPLC-RID, HPLC-ELSD, HPLC-DAD, GC-FID, GC-ECD, GC-Headspace, Karl Fisher
  • Titrations, FTIR, Kinematic Viscosity, Viscosity by Stabinger, Rotary Vap, Vacuum Ovens, NIR
  • Aseptic Microbiological testing utilizing traditional methods as well as Celsis instrument
  • Help write and revise SOP's or Analytical methods
  • Help establish ISO 9001, BRC, FSSC 22000, and Kosher in conjunction with Quality Assurance to attain certification.

Education

Associate of Arts Degree - Chemistry

Lake Superior College
Duluth, MN

Skills

  • Excellent computer skills and strong verbal/written communication skills
  • Good PC skills including experience with Microsoft Office
  • Demonstrated interpersonal and effective communication skills both verbal and written
  • Aseptic testing and sterile manufacturing
  • Extensive Deviations, Investigations, and CAPA experience
  • Solid problem-solving skills and ability to multi-task
  • Communicate effectively with various skill levels including technical, clinical, and non-clinical staff, directors, and managers
  • Effective Leadership skills, with the ability to motivate employees to meet and exceed performance expectations and recognize star performers

Certification

  • FSPCA
  • PCQI

Training

  • Chemistry I & II
  • Organic Chemistry I & II
  • Physics with Calculus I & II
  • Biology
  • Cell Biology
  • Calculus I, II & III
  • Differential Equations
  • Proteomics
  • Genomics

Timeline

QC Chemistry Supervisor

Catalent
08.2023 - 03.2024

QC Biochemistry Supervisor (Nights)

Lonza Pharmaceuticals
04.2022 - 07.2023

Supervisor, Chemistry

Alcami Corporation
04.2021 - 04.2022

QC Lab Supervisor API

Ani Pharmaceutical Inc
12.2019 - 04.2021

QC Laboratory Supervisor

Oxiteno USA LLC
12.2014 - 02.2019

Associate of Arts Degree - Chemistry

Lake Superior College

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