SPS US Investigator

The Investigator

is responsible to lead, conduct and document investigations relating to non-conformances and/or complaints

within a GMP Pharmaceutical packaging organization. The Investigator will utilize root cause analysis tools, critical thinking, and interviewing techniques to determine the root and contributing causal factors of

non-conformances/complaints.

The Investigator will offer recommendations to correct and/or prevent recurrence through CAPA design from the root cause conclusion of the investigation. The Investigator will lead, as necessary, the implementation of associated corrective and preventative actions through collaboration, teamwork, and influence. The position will

work closely and in collaboration with internal and occasionally external stakeholders.

The Investigator also has responsibilities for data generation, process evaluation and performance metrics for the purposes of customer communication and driving continuous improvement.
Must possess a working knowledge of FDA regulations pertaining to Pharmaceutical /Pharmaceutical Packaging Operations and a high level for detail and accuracy.
Scope of the position includes Allentown, Macungie and/or Conshohocken. The impact of decisions relating to customer interface, investigation conclusions, and documentation supporting recommendations for product impact assessments could expose the company to significant risk or economic loss.
ESSENTIAL DUTIES AND

RESPONSIBILITIES:

The following is a list of minimum responsibilities for the Investigator. Other duties may also be assigned.
Identifies issues and can independently assess the need for non-conformance and formulate recommended containment actions

in conjunction with operational leadership.
Conduct investigations that identify robust root cause by effectively applying root cause analysis tools across a variety of non-conformance and/or complaint types.
Independently lead and/or facilitate floor gembas, cross functional meetings, and operator interviews related to investigations.
Observe processes on shop floor, warehouse, and central support functions (incoming inspection, sales, customer service, project management, validation, and engineering) to ensure investigation is factual and detailed.
Author investigation reports in designated QMS utilizing strong organizational and technical writing skills with demonstrated attention to detail.
Lead effective cross-functional root cause analysis and CAPA and Continuous Improvement planning and execution with minimal supervision.
Owns data collection and performance metrics relative to the investigation process and CAPA effectiveness and facilitates sharing of investigational findings and risk knowledge through the organization.
Initiates, writes, reviews, and assesses change controls and revises SOPs and Work Instructions as needed for action implementation.
Utilizes knowledge, experience, and critical thinking skills to recommend potential product impact outcomes and provides thorough supporting documentation and justification for those outcomes.
Ability to thrive in a dynamic environment, multi-task, and independently prioritize and manage timelines to support packaging schedule, product disposition and release in alignment with organizational and customer goals.
Supports customer relationships related to investigation findings, CAPA implementation and performance metrics and process improvements.
Supports customer and regulatory audits as needed by presenting investigation summary and conclusions in a thoughtful, clear, and concise manner.
Lead continuous improvement efforts focused on investigation related processes or the reduction and/or elimination of organizational risk by closing GMP gaps.
Complete QMS actions related to change controls, non-conformance, complaints and CAPAs.
Proactively identify and facilitate resolution of potential risks.
Must be flexible to meet the needs to the organization when required.
SUPERVISORY RESPONSIBILITIES:
None
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
REQUIREMENTS:
Due to the nature of our work, all employees must be over the age of 18 and will be required to undergo a pre-employment drug test and background check.
EDUCATION and/or EXPERIENCE:
Bachelor’s degree is preferred with one to three years related experience or Associate’s Degree with three to five years of related experience. Experience in the packaging or inspection of pharmaceutical products or related industry is required.

Experience in the design, documentation, operation, maintenance, and/or improvement of biopharma facilities is preferred.

Outside certification of quality skills and practices (i.e., ASQ, CQIA, CQI, CQT, Lean Six Sigma etc.) is highly desired.
MATHEMATICAL SKILLS:
Ability to apply moderately complex mathematical operations including an understanding of statistical skills.
LANGUAGE SKILLS:
Ability to effectively communicate (written and verbally) with the following groups:
Internal Communication: Quality, Operations, Sales, Customer Service, Project Management, Validation, and Engineering teams.
External Communication: Represents Quality as the subject matter expert (SME) for customers and regulatory agencies on Investigations related non-conforming events.
WRITTEN SKILLS:
High level of writing and verbal skills, ability to provide clear, concise, and legible communication within investigation reports, internal and external correspondence, such as memos to file, electronic mail and investigation reports and procedure writing.
REASONING ABILITY:
Ability to independently make rational decisions pertaining to objective root cause and CAPA is required. Ability to trouble shoot and resolve problems effectively and efficiently. Ability to think critically about an issue and ask pertinent questions.
COMPUTER SKILLS:
Intermediate Windows applications including the Microsoft Office Suite and electronic QMS.
PHYSICAL DEMANDS:
The physical demands described here 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.
While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel and talk or hear. The employee frequently is required to sit. The employee is occasionally required to stand, walk, and reach with hands and arms. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus.
WORK ENVIRONMENT:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is normally required to sit at a desk or periodically go onto the shop floor. The working environment is clean and not normally subject to hazardous environment or conditions.
About Us

Sharp Packaging Services works across the world to create unique commercial and clinical packaging solutions for the pharmaceutical and biotechnology industry.
We are made up of two dynamic international divisions, Sharp Packaging Solutions and Sharp Clinical Services. Together our 1,600-strong team works from state-of-the-art facilities in the United States, United Kingdom, Belgium and the Netherlands.
We’ve built an exceptional global reputation for the design, serialisation and production of innovative, cost-effective compliance packaging for even the most complex products.
Our extensive range includes blister packs, bottles, pouches and stick packs, but our expertise goes far beyond, enabling us to support your product through every stage of design, development, manufacture and delivery.
Our clinical services division is one of the world’s leading providers of innovative clinical supply chain services, with a talented and highly experienced team that can handle every aspect of your supply chain. Our work spans everything from drug development and manufacturing to clinical supplies packaging, labelling, distribution, Qualified Person auditing and comparator sourcing.

#J-18808-Ljbffr