QCFS Manufacturing - VN 3rd Shift
A collective energy and ambition. A place where you can make a real difference.
We’re a company that genuinely cares about our people, our products, our consumers and the environment.
Our unique, informal culture champions courage, determination and collaboration. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work hard, innovate and push boundaries.
United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win.
Under general supervision, this position performs specialized and routine production inspection activities according to established Standard Operating Procedures and Good Manufacturing Practices requirements.
DUTIES AND RESPONSIBLITIES:
Following Standard Operating Procedures (SOP), company policies, safety policies and practices, quality standards, and Good Manufacturing Practices (GMP).
Providing assistance for all questions regarding quality defects.
Auditing all areas for quality and GMP conformance.
Ensuring batch documentation is filled out according to requirements.
Updating and completing documentation and logs as required, including observation reports.
Photocopying, sorting, and/or filing documents or reports as requested.
Informing Quality Control (QC) Shift Lead or Manager on all personnel issues.
Identifying and implementing improvements to the QC procedures as needed.
Performing the following according to exact established procedures:
Pack out quality
Lot and Code dates
Demonstrating a working knowledge of production equipment (processing and pack out equipment) and its related impact to overall quality.
Identifying urgent quality situations, assessing the nature of the problem then containing, resolving, or recommending action quickly.
Ensuring all personnel in the clean rooms and production areas are wearing the proper attire.
Ensuring proper cleaning is performed prior to next production run.
Ensuring the line clearance inspection is performed and documented before each production run and inspecting the production area to ensure that all components from previous run are removed before another production run is started.
Checking the Equipment Use Log to ensure it is correctly and completely filled out before each production run.
Verifying that the components match on the Work Order, Bill of Materials (BOM), and actual kit.
Stopping the lines immediately if a discrepancy is found, contacts the QC Shift Lead or Manager and helping to perform an investigation.
Pulling quality samples, in a sanitary manner, at all applicable production steps which include but is not limited to hot vitamin slurry as well as bulk product.
Calibrating or verifying all quality equipment.
Monitoring the dry rooms using a basic understanding of the SCADA system.
Performing other duties as required.
MINIMUM JOB REQUIREMENTS:
High school diploma, GED, and/or any equivalent combination of experience and education that could likely provide the required knowledge, skills, and abilities needed to perform the job. Previous QC experience in an FDA regulated industry preferred. A basic understanding of the SCADA system for dry room monitoring is required.
KNOWLEDGE, SKILLS, AND ABILITIES:
Ability to read, understand, and carry out oral and written instructions.
Ability to establish and maintain effective working relationships with others.
Ability to analyze complex quality system requirements and handle multiple tasks.
Ability to sort, check, count, and verify numbers.
Ability to prepare routine administrative documentation.
Ability to receive, track, and distribute materials, supplies, and equipment.
Ability to detect quality problems and report information to appropriate personnel.
Ability to maintain quality, safety, and/or infection control standards.
Good problem-solving skills.
Good interpersonal, verbal, and written communication skills.
Ability to define problems, collect data, and establish facts rather than opinions.
Ability to comply with standards and procedures.
Good understanding of 21 CFR 111 GMP for Dietary Supplements and NSF –ANSI 173.
Ability to maintain punctuality and predictable attendance.
Annual Current Good Manufacturing Practices (cGMP)
Annual Safety Training
Battery Acid –MSDS
Code of Conduct
Role specific training as indicated in the plant Training Tracker and/or Safety Matrix
Sexual Harassment Avoidance
Vitamin D3 in Corn Oil – MSDS
Must wear appropriate personal protective equipment and clean room attire.
Moderate physical activity, requires standing and/or walking for more than four (4) hours per day and up to twelve (12) hours per shift.
Must be able to lift and carry items weighing 50 pounds.
Must be able to perform work onsite and be comfortable in a light industrial environment, including some exposure to non-toxic dust.
Church & Dwight is proud to be an Equal Opportunity Employer/Veterans/Individuals with Disabilities.
For more information on our company, our brands and our culture visit us at http://www.churchdwight.com/
With corporate offices and major plants across the country, we’re building consumer products and connecting with global offices from the place where it all began.Explore this location
DIVERSITY At Church & Dwight
Church & Dwight strives to create an environment where everyone feels free to bring their authentic self to work every day.
We win when we respect every employee for who they are – regardless of gender, age, race, ethnicity, religion, disability, veteran status, sexual orientation or any other differences. We believe that our employees’ contributions are richer because of their diversity. We aim to be a diverse, inclusive and equitable company and are determined to build a culture where people have the power to win together.
CULTURE At Church & Dwight
We care - about our people, our products, our consumers and our environment. To honor these priorities, we’ve built our culture around the tenants of courage, determination and team spirit. We’re united by our small company feel and inspired by opportunities to make our mark.Learn More
Equal Employment Opportunity for the Disabled At Church & Dwight
As an equal opportunity employer, Church & Dwight is committed to providing access and opportunities to individuals with disabilities. Applicants who require accommodation in the job application process may contact 877-809-8449 or email their resume and cover letter to email@example.com. Please note that these options are available only to those needing an accommodation because of a medical condition or disability. All email submissions should include “Accommodation needed” in the subject line as well as information related to the specific position you are interested in (requisition number, job title, location, etc.). Church & Dwight will not respond to inquiries made to firstname.lastname@example.org or 877-809-8449 that are not related to accessibility of the online application system by persons with medical conditions or disabilities. To review Church & Dwight’s Equal Opportunities Employer Policy, click link below.Learn More