Brennan v. Cephalon, Inc.

298 F. App'x 147
CourtCourt of Appeals for the Third Circuit
DecidedOctober 7, 2008
Docket07-2702
StatusUnpublished
Cited by7 cases

This text of 298 F. App'x 147 (Brennan v. Cephalon, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Third Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Brennan v. Cephalon, Inc., 298 F. App'x 147 (3d Cir. 2008).

Opinion

OPINION

BARRY, Circuit Judge.

In this case of alleged wrongful termination, David Brennan appeals the order of the District Court granting summary judgment to his former employer, Cephalon, Inc. (“Cephalon”). We have jurisdiction under 28 U.S.C. § 1291, and will affirm.

I.

Cephalon is a biotechnology and drug company. In 2000, it acquired Anesta Corp., the developer and manufacturer of Actiq, a prescription opioid designed to treat cancer pain. As a condition of the Food and Drug Administration’s (“FDA”) approval of Actiq, Anesta agreed to a Risk Management Program (“RMP”). The RMP contains strict guidelines for the labeling, packaging, and marketing of Actiq. It also requires that Cephalon monitor and tabulate certain patient, prescription, and usage information and regularly report this information to the FDA.

In 2003, Brennan, an at-will employee, was assigned to audit Cephalon’s compliance with the terms and conditions of the Actiq RMP. In October 2003, he prepared a report in which he concluded that Cephalon was not in compliance in various respects. Several times over the next six weeks, Brennan asked his supervisor, Cephalon’s Assistant Director of Quality Assurance Tim Sheehan, for permission to distribute the report internally; Sheehan repeatedly refused to grant permission. Frustrated with what he perceived as a lack of action, Brennan told a co-worker on November 10, 2003 that he planned to submit his audit report directly to the FDA. This co-worker suggested that *149 Brennan first speak to Cephalon’s new Director of Quality Assurance — and Sheehan’s direct supervisor — Armando Cortez. Brennan did so.

After Brennan spoke to Cortez, Cortez held a meeting on November 18, 2003 with Brennan, Sheehan, and Richard Kaplan, Cephalon’s Vice President of Quality and Environmental Health and Safety. At that meeting, Kaplan told Brennan to mark his report “Confidential” and to organize a meeting with other participants in the Actiq audit to verify his conclusions.

On December 1, 2003, Brennan met with several audit participants, including Tracie Parker, a non-supervisory employee in the Regulatory Affairs Department. Parker argued against reporting that Cephalon was not in compliance, instructed that her name be removed from the audit report, and left the meeting for several minutes before returning with Kaplan. Although Kaplan asked Brennan several questions, he did not tell Brennan to alter his report. After Kaplan and Parker left, Brennan was given suggestions by other audit participants. He incorporated several of the suggestions into his revised report, which reached the same conclusion as before— namely, that Cephalon was not in compliance with the Actiq RMP. Brennan circulated this report to the heads of several departments, including Carol Marchione, the Director of Regulatory Affairs, who was responsible for preparing the internal response to the RMP report.

Marchione called a meeting for December 11, 2003 to formulate a plan for addressing the deficiencies outlined in the report. The assembled employees, including Brennan, Sheehan, Cortez, Kaplan, and Parker, discussed options for corrective action. Marchione summarized the meeting in a memorandum dated December 15, 2003, and committed to a formal response by January 31, 2004. This deadline was not met.

On February 9, 2004 and on several days thereafter, Brennan spoke to Sheehan about the delay in responding to the report and proposed asking Marchione about her overdue response. Sheehan told Brennan to wait for approval from Cortez. By letters dated February 12, 2004, Cephalon terminated both Brennan and Sheehan. On or about February 19, 2004, Brennan sent a letter to the FDA disclosing Cephalon’s noncompliance with the Actiq RMP.

In March 2004, Marchione circulated a draft memorandum containing written responses to the problem areas identified in Brennan’s audit report and met with several employees to review this draft. On March 22, 2004, Marchione issued a memorandum with the final written responses to the RMP audit. At his deposition, Brennan testified that the March 22 memorandum was the type of document he would have expected to see in response to his audit report. He also stated that the report “indicated that there was progress in complying with the requirements of the risk management program and complying with the reporting requirements to the FDA.” (SA 44.)

Cephalon maintains that Brennan’s termination had nothing to do with the Actiq RMP report but rather was prompted by his unsatisfactory performance during the November 2003 audit of Orsymonde, a Cephalon-owned manufacturing facility in France. It claims that a subsequent “mock FDA inspection” of that facility in December 2003 and January 2004 revealed several violations requiring corrective action that Brennan failed to detect only a few months earlier. The report of this mock inspection issued on February 6, 2004. Brennan’s termination notice, sent less than a week later, specifically referenced his poor performance during the Orsymonde audit. Cephalon gave the *150 same reason for its termination of Sheehan.

Brennan filed a complaint in June 2004 against Cephalon and several of its employees, raising a number of federal and state law claims. The gravamen of these claims was that he was discharged for (1) his insistence that Cephalon disclose the non-compliance data contained in the RMP report to the FDA or he would do so himself, and (2) his refusal to change his conclusion of non-compliance to compliance in his report. By orders dated March 2, 2005 and October 25, 2005, 2005 WL 2807195, the District Court dismissed all of Brennan’s claims with the exception of his wrongful discharge claim against Cephalon. 1

On May 8, 2007, 2007 WL 1382801, the District Court granted summary judgment in favor of Cephalon on Brennan’s wrongful termination claim. Specifically, the Court determined that Brennan’s termination did not fall under the public policy exception to Pennsylvania’s at-will employment doctrine because Brennan: (1) did not identify a statutorily imposed duty to report his employer’s non-compliance with the Actiq RMP; and (2) failed to adduce sufficient evidence that Cephalon directed him to falsify and/or conceal the results of his audit. Brennan now appeals.

II.

We exercise plenary review of grants of summary judgment. Ye v. United States, 484 F.3d 634, 636 (3d Cir.2007). Summary judgment is appropriate where “there is no genuine issue as to any material fact” and judgment may be granted as a matter of law. Fed.R.Civ.P. 56(c).

In Pennsylvania, an at-will employee generally can be terminated for any reason, with or without cause. Shiek v. Shirey, 552 Pa. 590, 716 A.2d 1231, 1233 (1998). An exception to this rule exists in limited circumstances where the termination violates a clear mandate of public policy. McLaughlin v. Gastrointestinal Specialists, Inc., 561 Pa.

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Bluebook (online)
298 F. App'x 147, Counsel Stack Legal Research, https://law.counselstack.com/opinion/brennan-v-cephalon-inc-ca3-2008.