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Sr Quality Partner
1080 US Highway 202 South Branchburg, NJ 08876 US
Job Description
Target Pay Rate: 30-36.12/hr **salary will be commensurate with experience
Job Description:
As an Operations Quality Senior Quality Partner you are accountable for ensuring your contributions are delivered in a way that lives up to our commitments to each other and the We Diagnostic Commitments. You are responsible for building and developing your capabilities to contribute more to the team, customers and patients. You apply new approaches to improving your work to increase productivity, reduce costs or mitigate significant compliance issues within your area of influence. You work as a strategic business partner to help break down silos between organizations (internal and external) all which lead to developing and producing safe, quality products and services that meet customer requirements throughout the entire lifecycle. You push the boundaries to enable and implement smart, risk-based compliant processes that result in quick and efficient innovation.
You will be responsible to 1. Drive business results and customer value a. Responsible for performing activities as required to meet Q&R goals and objectives independently. Able to identify improvements and implement with collaboration from your manager. b. Be recognized internally as an expert in your own job discipline with in-depth knowledge/skill-set of related disciplines in the field. c. Act as a coach for colleagues with less experience and help them develop skills/expertise. d. Document authoring and review as required to support changes. Performs technical reviews, as applicable. May require collaboration with supervisor on technically complex technical reviews independently. e. Preparing documentation for and participating in audits as applicable. f. Completing all required training in learning solution. g. Responsible for training, coaching and mentoring other quality managers or business partners, as applicable in a professional manner to ensure that business needs are being met. h. Able to troubleshoot issues as they arise, develop and independently implement solutions to ensure that daily work is completed without jeopardizing compliance. i. Communicating significant quality or regulatory issues and risks that may impact product quality or regulatory compliance in a timely manner to Executive Management.
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Advance the work of the Network, making tradeoffs and breaking silos a. Ability to work day to day with minimal to no supervision to correctly complete daily scheduled and unscheduled activities. Initiates activities independently and initiates interactions across departments as applicable. Initiates daily activities independently. Has courage to make decisions even outside of scope/comfort zone. Is decisive and does not procrastinate on decisions; develop solutions and present both issues and solutions to your manager. b. Identify, Initiate, facilitate, participate and implement process improvements to meet business needs. Able to link responsibilities with both site and Global Quality and Regulatory. Drive innovation across the local organization/site. c. Leads or contributes with skills to projects / squads within. d. Participates in large/global cross-functional or cross-chapter projects. e. Be involved in solving unique or unprecedented problems that have an impact on a part of the organization, function or chapter.
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Empower and enable the Network a. Build and maintain strong partnerships with colleagues and business patterns to assure alignment around strategic projects and day-to-day activities and to assure mutually successful working relationships. b. Be the champion and advocate for Engrained Quality at the Site. c. Build a culture of continuous improvement.
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Enable the organizations New Ways of Working a. Act as role-model for Agile Leadership behaviors, as well as for our culture, mindset & behaviors as defined in the Dia Operating Principles b. Model behaviors to support the organizations transformation to new, more Agile Ways of Working - e.g. new decision making/governance practices, collaboration, etc. c. Everything you do should contribute directly to the achievement of our Ten Year ambitions, including:
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Double patient access to novel, high-medical-value diagnostics solutions
- Build the leading, profitable insights business
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Improve patients lives via Approach to ecosystem in every country How a. Know and follow the Dia Operating Principles and Core Competencies. Adopts and adheres to the Leadership Commitments. Accountable for meeting commitments. Is flexible and able to shift priorities while balancing commitments and daily work requirements, independently. Seeks candid feedback on his or her performance and acts on it. Recognizes the contributions of teammates and peers. Establishes strong collaborative relationships inter-departmentally and across the sites and leverages these connections to achieve our key results. Identifies personal goals and actively manages her or his career to pursue personal goals and priorities independently.
What else do you have in your toolbox:
- 3-5 years experience
- Bachelors / Master degree in Life Science, Data Science or related subject or equivalent experience. Completed training as a technician or laboratory technician; or equivalent qualification for the tasks; limited working experience.
- Has worked in more than one function within quality management and may have worked outside of Quality Management. Can managing highly complex and/or global projects, or equivalent experience.
Locations:
You are based in Branchburg.
At the Company's discretion, an exception to the location requirement could be made under extraordinary circumstances.
As this position is part of a global organization, international business travel will be required depending upon the business location of the successful candidate and ongoing business project activities.
Client is strongly committed to a diverse and inclusive workplace. We strive to build teams that represent a range of backgrounds, perspectives, and skills. Embracing diversity enables us to create a great place to work and to innovate for patients client is an equal opportunity employer
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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